<opt>
  <data id="7_100318423_duplication" allele_string="duplication" assembly_name="GRCh38" end="100321323" input="7 100318423 100321323 DUP 1" most_severe_consequence="feature_elongation" seq_region_name="7" start="100318423" strand="1">
    <transcript_consequences biotype="protein_coding" bp_overlap="2901" cdna_end="2312" gene_id="ENSG00000214300" gene_symbol="SPDYE3" gene_symbol_source="HGNC" hgnc_id="HGNC:35462" impact="HIGH" percentage_overlap="20.01" strand="1" transcript_id="ENST00000332397" variant_allele="duplication">
      <consequence_terms>feature_elongation</consequence_terms>
      <consequence_terms>coding_sequence_variant</consequence_terms>
      <consequence_terms>3_prime_UTR_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="retained_intron" bp_overlap="2901" cdna_end="2092" gene_id="ENSG00000214300" gene_symbol="SPDYE3" gene_symbol_source="HGNC" hgnc_id="HGNC:35462" impact="HIGH" percentage_overlap="36.57" strand="1" transcript_id="ENST00000380765" variant_allele="duplication">
      <consequence_terms>feature_elongation</consequence_terms>
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="413" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.74" strand="-1" transcript_id="ENST00000674842" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" distance="2830" gene_id="ENSG00000291178" impact="MODIFIER" strand="-1" transcript_id="ENST00000674972" variant_allele="duplication">
      <consequence_terms>downstream_gene_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="885" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="7.31" strand="-1" transcript_id="ENST00000674981" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="2436" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="13.93" strand="-1" transcript_id="ENST00000675162" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="2432" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="13.92" strand="-1" transcript_id="ENST00000675610" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" distance="4334" gene_id="ENSG00000291178" impact="MODIFIER" strand="-1" transcript_id="ENST00000675620" variant_allele="duplication">
      <consequence_terms>downstream_gene_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="411" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.73" strand="-1" transcript_id="ENST00000675639" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" distance="4334" gene_id="ENSG00000291178" impact="MODIFIER" strand="-1" transcript_id="ENST00000675640" variant_allele="duplication">
      <consequence_terms>downstream_gene_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="415" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.75" strand="-1" transcript_id="ENST00000676155" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="828" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="5.37" strand="-1" transcript_id="ENST00000676198" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="2102" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="12.26" strand="-1" transcript_id="ENST00000676200" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="825" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="5.35" strand="-1" transcript_id="ENST00000676204" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="885" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="5.71" strand="-1" transcript_id="ENST00000676241" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="retained_intron" bp_overlap="409" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="4.63" strand="-1" transcript_id="ENST00000676256" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="2433" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="14.24" strand="-1" transcript_id="ENST00000676274" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" distance="4334" gene_id="ENSG00000291178" impact="MODIFIER" strand="-1" transcript_id="ENST00000685342" variant_allele="duplication">
      <consequence_terms>downstream_gene_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="411" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.73" strand="-1" transcript_id="ENST00000685473" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="411" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.73" strand="-1" transcript_id="ENST00000685499" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="2901" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="8.07" strand="-1" transcript_id="ENST00000685541" variant_allele="duplication">
      <consequence_terms>intron_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" distance="4337" gene_id="ENSG00000291178" impact="MODIFIER" strand="-1" transcript_id="ENST00000685607" variant_allele="duplication">
      <consequence_terms>downstream_gene_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="411" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.73" strand="-1" transcript_id="ENST00000685670" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="411" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.74" strand="-1" transcript_id="ENST00000685700" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="2901" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="8.07" strand="-1" transcript_id="ENST00000685724" variant_allele="duplication">
      <consequence_terms>intron_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="411" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.74" strand="-1" transcript_id="ENST00000685805" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="413" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.74" strand="-1" transcript_id="ENST00000685852" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="418" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.77" strand="-1" transcript_id="ENST00000685901" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="981" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="6.27" strand="-1" transcript_id="ENST00000686203" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" distance="4336" gene_id="ENSG00000291178" impact="MODIFIER" strand="-1" transcript_id="ENST00000686569" variant_allele="duplication">
      <consequence_terms>downstream_gene_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" distance="4334" gene_id="ENSG00000291178" impact="MODIFIER" strand="-1" transcript_id="ENST00000686594" variant_allele="duplication">
      <consequence_terms>downstream_gene_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="421" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.79" strand="-1" transcript_id="ENST00000686797" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" distance="4336" gene_id="ENSG00000291178" impact="MODIFIER" strand="-1" transcript_id="ENST00000686825" variant_allele="duplication">
      <consequence_terms>downstream_gene_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="988" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="6.32" strand="-1" transcript_id="ENST00000686838" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="413" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.74" strand="-1" transcript_id="ENST00000686890" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" distance="4260" gene_id="ENSG00000291178" impact="MODIFIER" strand="-1" transcript_id="ENST00000687026" variant_allele="duplication">
      <consequence_terms>downstream_gene_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" distance="4334" gene_id="ENSG00000291178" impact="MODIFIER" strand="-1" transcript_id="ENST00000687053" variant_allele="duplication">
      <consequence_terms>downstream_gene_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="984" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="6.14" strand="-1" transcript_id="ENST00000687177" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="2429" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="13.93" strand="-1" transcript_id="ENST00000687616" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="411" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.74" strand="-1" transcript_id="ENST00000687713" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="411" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.73" strand="-1" transcript_id="ENST00000687801" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="415" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.76" strand="-1" transcript_id="ENST00000688104" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="413" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.74" strand="-1" transcript_id="ENST00000688544" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="416" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.76" strand="-1" transcript_id="ENST00000689000" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="410" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.73" strand="-1" transcript_id="ENST00000689019" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="413" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.74" strand="-1" transcript_id="ENST00000689267" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="411" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.73" strand="-1" transcript_id="ENST00000689447" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" distance="4336" gene_id="ENSG00000291178" impact="MODIFIER" strand="-1" transcript_id="ENST00000689538" variant_allele="duplication">
      <consequence_terms>downstream_gene_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="981" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="6.29" strand="-1" transcript_id="ENST00000689609" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="413" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.74" strand="-1" transcript_id="ENST00000689719" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="655" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="4.18" strand="-1" transcript_id="ENST00000689817" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="413" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.74" strand="-1" transcript_id="ENST00000689907" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="415" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.75" strand="-1" transcript_id="ENST00000690446" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" distance="4333" gene_id="ENSG00000291178" impact="MODIFIER" strand="-1" transcript_id="ENST00000690914" variant_allele="duplication">
      <consequence_terms>downstream_gene_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="409" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.73" strand="-1" transcript_id="ENST00000690988" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="415" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.75" strand="-1" transcript_id="ENST00000691046" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" distance="4133" gene_id="ENSG00000291178" impact="MODIFIER" strand="-1" transcript_id="ENST00000691107" variant_allele="duplication">
      <consequence_terms>downstream_gene_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="590" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="3.88" strand="-1" transcript_id="ENST00000691110" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="413" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.75" strand="-1" transcript_id="ENST00000691247" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="413" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.74" strand="-1" transcript_id="ENST00000691275" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="1023" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="6.36" strand="-1" transcript_id="ENST00000691424" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="411" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.74" strand="-1" transcript_id="ENST00000691428" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" distance="4337" gene_id="ENSG00000291178" impact="MODIFIER" strand="-1" transcript_id="ENST00000691660" variant_allele="duplication">
      <consequence_terms>downstream_gene_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="413" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.74" strand="-1" transcript_id="ENST00000691707" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="411" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.74" strand="-1" transcript_id="ENST00000691816" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" distance="4337" gene_id="ENSG00000291178" impact="MODIFIER" strand="-1" transcript_id="ENST00000691842" variant_allele="duplication">
      <consequence_terms>downstream_gene_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="413" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.74" strand="-1" transcript_id="ENST00000691905" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="413" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.75" strand="-1" transcript_id="ENST00000691910" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" distance="4334" gene_id="ENSG00000291178" impact="MODIFIER" strand="-1" transcript_id="ENST00000692231" variant_allele="duplication">
      <consequence_terms>downstream_gene_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="422" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.73" strand="-1" transcript_id="ENST00000692261" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="2901" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="8.06" strand="-1" transcript_id="ENST00000692351" variant_allele="duplication">
      <consequence_terms>intron_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" distance="4337" gene_id="ENSG00000291178" impact="MODIFIER" strand="-1" transcript_id="ENST00000692675" variant_allele="duplication">
      <consequence_terms>downstream_gene_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="413" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.67" strand="-1" transcript_id="ENST00000692687" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" distance="4337" gene_id="ENSG00000291178" impact="MODIFIER" strand="-1" transcript_id="ENST00000692752" variant_allele="duplication">
      <consequence_terms>downstream_gene_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="411" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.73" strand="-1" transcript_id="ENST00000692947" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="415" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.75" strand="-1" transcript_id="ENST00000693010" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="1009" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="6.3" strand="-1" transcript_id="ENST00000693042" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="988" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="6.16" strand="-1" transcript_id="ENST00000693192" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
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    <transcript_consequences biotype="lncRNA" bp_overlap="415" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.69" strand="-1" transcript_id="ENST00000693215" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
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    <transcript_consequences biotype="lncRNA" bp_overlap="411" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.74" strand="-1" transcript_id="ENST00000693302" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="413" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.67" strand="-1" transcript_id="ENST00000693490" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="415" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.75" strand="-1" transcript_id="ENST00000700850" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" distance="4320" gene_id="ENSG00000291178" impact="MODIFIER" strand="-1" transcript_id="ENST00000700905" variant_allele="duplication">
      <consequence_terms>downstream_gene_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="411" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.74" strand="-1" transcript_id="ENST00000701011" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="411" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.73" strand="-1" transcript_id="ENST00000701138" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
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    <transcript_consequences biotype="lncRNA" bp_overlap="2901" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="8.08" strand="-1" transcript_id="ENST00000701204" variant_allele="duplication">
      <consequence_terms>intron_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_variant</consequence_terms>
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    <transcript_consequences biotype="lncRNA" bp_overlap="411" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.74" strand="-1" transcript_id="ENST00000701582" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
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    <transcript_consequences biotype="lncRNA" bp_overlap="411" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.74" strand="-1" transcript_id="ENST00000701649" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
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    <transcript_consequences biotype="lncRNA" bp_overlap="411" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.73" strand="-1" transcript_id="ENST00000701653" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="411" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.75" strand="-1" transcript_id="ENST00000701849" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
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    <transcript_consequences biotype="lncRNA" bp_overlap="413" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.74" strand="-1" transcript_id="ENST00000701970" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" distance="4337" gene_id="ENSG00000291178" impact="MODIFIER" strand="-1" transcript_id="ENST00000702039" variant_allele="duplication">
      <consequence_terms>downstream_gene_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="2901" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="8.08" strand="-1" transcript_id="ENST00000702062" variant_allele="duplication">
      <consequence_terms>intron_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_variant</consequence_terms>
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    <transcript_consequences biotype="lncRNA" bp_overlap="413" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.74" strand="-1" transcript_id="ENST00000702164" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
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    <transcript_consequences biotype="lncRNA" bp_overlap="411" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.73" strand="-1" transcript_id="ENST00000702228" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" distance="4335" gene_id="ENSG00000291178" impact="MODIFIER" strand="-1" transcript_id="ENST00000702250" variant_allele="duplication">
      <consequence_terms>downstream_gene_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="411" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.73" strand="-1" transcript_id="ENST00000702364" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="411" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.67" strand="-1" transcript_id="ENST00000702448" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
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    <transcript_consequences biotype="lncRNA" distance="4337" gene_id="ENSG00000291178" impact="MODIFIER" strand="-1" transcript_id="ENST00000702527" variant_allele="duplication">
      <consequence_terms>downstream_gene_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="411" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.74" strand="-1" transcript_id="ENST00000702566" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
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    <transcript_consequences biotype="lncRNA" bp_overlap="936" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="6.01" strand="-1" transcript_id="ENST00000702596" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
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    <transcript_consequences biotype="lncRNA" bp_overlap="411" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.74" strand="-1" transcript_id="ENST00000702608" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
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    <transcript_consequences biotype="lncRNA" bp_overlap="411" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.73" strand="-1" transcript_id="ENST00000702615" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
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    <transcript_consequences biotype="lncRNA" bp_overlap="410" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.73" strand="-1" transcript_id="ENST00000702718" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
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    <transcript_consequences biotype="lncRNA" bp_overlap="2901" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="9.66" strand="-1" transcript_id="ENST00000702720" variant_allele="duplication">
      <consequence_terms>intron_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_variant</consequence_terms>
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    <transcript_consequences biotype="lncRNA" distance="4337" gene_id="ENSG00000291178" impact="MODIFIER" strand="-1" transcript_id="ENST00000702773" variant_allele="duplication">
      <consequence_terms>downstream_gene_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" distance="4337" gene_id="ENSG00000291178" impact="MODIFIER" strand="-1" transcript_id="ENST00000702822" variant_allele="duplication">
      <consequence_terms>downstream_gene_variant</consequence_terms>
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    <transcript_consequences biotype="lncRNA" distance="4336" gene_id="ENSG00000291178" impact="MODIFIER" strand="-1" transcript_id="ENST00000702891" variant_allele="duplication">
      <consequence_terms>downstream_gene_variant</consequence_terms>
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    <transcript_consequences biotype="lncRNA" bp_overlap="2901" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="5.05" strand="-1" transcript_id="ENST00000718500" variant_allele="duplication">
      <consequence_terms>intron_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_variant</consequence_terms>
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    <transcript_consequences biotype="lncRNA" bp_overlap="2901" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="5.49" strand="-1" transcript_id="ENST00000718501" variant_allele="duplication">
      <consequence_terms>intron_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_variant</consequence_terms>
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    <transcript_consequences biotype="lncRNA" bp_overlap="2901" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="5.92" strand="-1" transcript_id="ENST00000718502" variant_allele="duplication">
      <consequence_terms>intron_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_variant</consequence_terms>
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    <transcript_consequences biotype="lncRNA" bp_overlap="2901" gene_id="ENSG00000293698" impact="MODIFIER" percentage_overlap="2.57" strand="-1" transcript_id="ENST00000842201" variant_allele="duplication">
      <consequence_terms>intron_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_variant</consequence_terms>
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    <transcript_consequences biotype="lncRNA" bp_overlap="2901" gene_id="ENSG00000293698" impact="MODIFIER" percentage_overlap="2.57" strand="-1" transcript_id="ENST00000842202" variant_allele="duplication">
      <consequence_terms>intron_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_variant</consequence_terms>
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    <transcript_consequences biotype="lncRNA" bp_overlap="2901" gene_id="ENSG00000293698" impact="MODIFIER" percentage_overlap="2.57" strand="-1" transcript_id="ENST00000842203" variant_allele="duplication">
      <consequence_terms>intron_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_variant</consequence_terms>
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    <transcript_consequences biotype="lncRNA" bp_overlap="2901" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="4.8" strand="-1" transcript_id="ENST00000843375" variant_allele="duplication">
      <consequence_terms>intron_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_variant</consequence_terms>
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    <transcript_consequences biotype="lncRNA" bp_overlap="2901" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="5.04" strand="-1" transcript_id="ENST00000843376" variant_allele="duplication">
      <consequence_terms>intron_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_variant</consequence_terms>
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    <transcript_consequences biotype="lncRNA" bp_overlap="2901" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="5.04" strand="-1" transcript_id="ENST00000843377" variant_allele="duplication">
      <consequence_terms>intron_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_variant</consequence_terms>
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    <transcript_consequences biotype="lncRNA" bp_overlap="2901" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="5.49" strand="-1" transcript_id="ENST00000843378" variant_allele="duplication">
      <consequence_terms>intron_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_variant</consequence_terms>
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    <transcript_consequences biotype="lncRNA" bp_overlap="2901" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="5.49" strand="-1" transcript_id="ENST00000843379" variant_allele="duplication">
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      <consequence_terms>non_coding_transcript_variant</consequence_terms>
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    <transcript_consequences biotype="lncRNA" bp_overlap="2901" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="5.53" strand="-1" transcript_id="ENST00000843380" variant_allele="duplication">
      <consequence_terms>intron_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_variant</consequence_terms>
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    <transcript_consequences biotype="lncRNA" bp_overlap="2901" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="5.53" strand="-1" transcript_id="ENST00000843381" variant_allele="duplication">
      <consequence_terms>intron_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_variant</consequence_terms>
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    <transcript_consequences biotype="lncRNA" bp_overlap="2901" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="5.53" strand="-1" transcript_id="ENST00000843382" variant_allele="duplication">
      <consequence_terms>intron_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_variant</consequence_terms>
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    <transcript_consequences biotype="lncRNA" bp_overlap="2901" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="5.53" strand="-1" transcript_id="ENST00000843383" variant_allele="duplication">
      <consequence_terms>intron_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_variant</consequence_terms>
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    <transcript_consequences biotype="lncRNA" bp_overlap="2901" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="5.53" strand="-1" transcript_id="ENST00000843384" variant_allele="duplication">
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      <consequence_terms>non_coding_transcript_variant</consequence_terms>
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    <transcript_consequences biotype="lncRNA" bp_overlap="2901" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="5.53" strand="-1" transcript_id="ENST00000843385" variant_allele="duplication">
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      <consequence_terms>non_coding_transcript_variant</consequence_terms>
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    <transcript_consequences biotype="lncRNA" bp_overlap="2901" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="5.53" strand="-1" transcript_id="ENST00000843386" variant_allele="duplication">
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    <transcript_consequences biotype="lncRNA" bp_overlap="2901" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="5.53" strand="-1" transcript_id="ENST00000843387" variant_allele="duplication">
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      <consequence_terms>non_coding_transcript_variant</consequence_terms>
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    <transcript_consequences biotype="lncRNA" bp_overlap="2901" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="5.53" strand="-1" transcript_id="ENST00000843388" variant_allele="duplication">
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    <transcript_consequences biotype="lncRNA" bp_overlap="2901" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="5.53" strand="-1" transcript_id="ENST00000843389" variant_allele="duplication">
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    <transcript_consequences biotype="lncRNA" bp_overlap="2901" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="5.54" strand="-1" transcript_id="ENST00000843390" variant_allele="duplication">
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    <transcript_consequences biotype="lncRNA" bp_overlap="2901" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="5.54" strand="-1" transcript_id="ENST00000843392" variant_allele="duplication">
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    <transcript_consequences biotype="lncRNA" bp_overlap="2901" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="5.93" strand="-1" transcript_id="ENST00000843393" variant_allele="duplication">
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    <transcript_consequences biotype="lncRNA" bp_overlap="2901" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="7.1" strand="-1" transcript_id="ENST00000843394" variant_allele="duplication">
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    <transcript_consequences biotype="lncRNA" bp_overlap="2901" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="7.1" strand="-1" transcript_id="ENST00000843395" variant_allele="duplication">
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      <consequence_terms>non_coding_transcript_variant</consequence_terms>
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    <transcript_consequences biotype="lncRNA" bp_overlap="2901" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="8.07" strand="-1" transcript_id="ENST00000843398" variant_allele="duplication">
      <consequence_terms>intron_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="2901" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="8.08" strand="-1" transcript_id="ENST00000843399" variant_allele="duplication">
      <consequence_terms>intron_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="2901" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="8.08" strand="-1" transcript_id="ENST00000843400" variant_allele="duplication">
      <consequence_terms>intron_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="2901" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="8.08" strand="-1" transcript_id="ENST00000843401" variant_allele="duplication">
      <consequence_terms>intron_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="2901" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="8.08" strand="-1" transcript_id="ENST00000843402" variant_allele="duplication">
      <consequence_terms>intron_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_variant</consequence_terms>
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    <transcript_consequences biotype="lncRNA" bp_overlap="2901" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="8.08" strand="-1" transcript_id="ENST00000843403" variant_allele="duplication">
      <consequence_terms>intron_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="2901" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="8.11" strand="-1" transcript_id="ENST00000843404" variant_allele="duplication">
      <consequence_terms>intron_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="2901" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="9.26" strand="-1" transcript_id="ENST00000843405" variant_allele="duplication">
      <consequence_terms>intron_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="2901" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="9.42" strand="-1" transcript_id="ENST00000843406" variant_allele="duplication">
      <consequence_terms>intron_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="2901" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="9.51" strand="-1" transcript_id="ENST00000843407" variant_allele="duplication">
      <consequence_terms>intron_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="2901" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="9.51" strand="-1" transcript_id="ENST00000843408" variant_allele="duplication">
      <consequence_terms>intron_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_variant</consequence_terms>
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    <transcript_consequences biotype="lncRNA" bp_overlap="2901" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="9.51" strand="-1" transcript_id="ENST00000843409" variant_allele="duplication">
      <consequence_terms>intron_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="2901" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="9.52" strand="-1" transcript_id="ENST00000843410" variant_allele="duplication">
      <consequence_terms>intron_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="2901" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="9.52" strand="-1" transcript_id="ENST00000843411" variant_allele="duplication">
      <consequence_terms>intron_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="2901" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="9.53" strand="-1" transcript_id="ENST00000843412" variant_allele="duplication">
      <consequence_terms>intron_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="2901" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="9.53" strand="-1" transcript_id="ENST00000843413" variant_allele="duplication">
      <consequence_terms>intron_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="2901" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="9.66" strand="-1" transcript_id="ENST00000843414" variant_allele="duplication">
      <consequence_terms>intron_variant</consequence_terms>
      <consequence_terms>non_coding_transcript_variant</consequence_terms>
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    <transcript_consequences biotype="lncRNA" bp_overlap="984" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="6.16" strand="-1" transcript_id="ENST00000843415" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="984" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="6.29" strand="-1" transcript_id="ENST00000843416" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="413" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.67" strand="-1" transcript_id="ENST00000843417" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="411" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.66" strand="-1" transcript_id="ENST00000843418" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="415" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.75" strand="-1" transcript_id="ENST00000843419" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="413" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.74" strand="-1" transcript_id="ENST00000843420" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="416" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.76" strand="-1" transcript_id="ENST00000843421" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="411" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.73" strand="-1" transcript_id="ENST00000843422" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="413" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.74" strand="-1" transcript_id="ENST00000843423" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="411" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.73" strand="-1" transcript_id="ENST00000843424" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="413" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.74" strand="-1" transcript_id="ENST00000843425" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="413" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.74" strand="-1" transcript_id="ENST00000843426" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="413" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.74" strand="-1" transcript_id="ENST00000843427" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="413" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.74" strand="-1" transcript_id="ENST00000843428" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="411" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.73" strand="-1" transcript_id="ENST00000843429" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="411" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.73" strand="-1" transcript_id="ENST00000843430" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="415" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.76" strand="-1" transcript_id="ENST00000843431" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="411" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.73" strand="-1" transcript_id="ENST00000843432" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="411" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.73" strand="-1" transcript_id="ENST00000843433" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="413" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.74" strand="-1" transcript_id="ENST00000843434" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="413" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.74" strand="-1" transcript_id="ENST00000843435" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="411" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.73" strand="-1" transcript_id="ENST00000843436" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="411" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.73" strand="-1" transcript_id="ENST00000843437" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="413" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.74" strand="-1" transcript_id="ENST00000843438" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="407" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.7" strand="-1" transcript_id="ENST00000843439" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="411" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.73" strand="-1" transcript_id="ENST00000843440" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="411" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.73" strand="-1" transcript_id="ENST00000843441" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="411" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.73" strand="-1" transcript_id="ENST00000843442" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="411" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.73" strand="-1" transcript_id="ENST00000843443" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="411" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.73" strand="-1" transcript_id="ENST00000843444" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="411" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.73" strand="-1" transcript_id="ENST00000843445" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="411" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.73" strand="-1" transcript_id="ENST00000843446" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="410" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.73" strand="-1" transcript_id="ENST00000843447" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="413" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.75" strand="-1" transcript_id="ENST00000843448" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="411" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.73" strand="-1" transcript_id="ENST00000843449" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="411" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.73" strand="-1" transcript_id="ENST00000843450" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="411" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.73" strand="-1" transcript_id="ENST00000843451" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="411" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.74" strand="-1" transcript_id="ENST00000843452" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="411" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.74" strand="-1" transcript_id="ENST00000843453" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="413" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.75" strand="-1" transcript_id="ENST00000843454" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="413" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.75" strand="-1" transcript_id="ENST00000843455" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="411" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.74" strand="-1" transcript_id="ENST00000843456" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="411" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.74" strand="-1" transcript_id="ENST00000843457" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="411" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.74" strand="-1" transcript_id="ENST00000843458" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="411" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.74" strand="-1" transcript_id="ENST00000843459" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="411" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.74" strand="-1" transcript_id="ENST00000843460" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="411" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.74" strand="-1" transcript_id="ENST00000843461" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="411" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.74" strand="-1" transcript_id="ENST00000843462" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" bp_overlap="411" gene_id="ENSG00000291178" impact="MODIFIER" percentage_overlap="2.74" strand="-1" transcript_id="ENST00000843463" variant_allele="duplication">
      <consequence_terms>non_coding_transcript_exon_variant</consequence_terms>
      <consequence_terms>intron_variant</consequence_terms>
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      <consequence_terms>downstream_gene_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" distance="4337" gene_id="ENSG00000291178" impact="MODIFIER" strand="-1" transcript_id="ENST00000843542" variant_allele="duplication">
      <consequence_terms>downstream_gene_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" distance="4337" gene_id="ENSG00000291178" impact="MODIFIER" strand="-1" transcript_id="ENST00000843543" variant_allele="duplication">
      <consequence_terms>downstream_gene_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" distance="4337" gene_id="ENSG00000291178" impact="MODIFIER" strand="-1" transcript_id="ENST00000843544" variant_allele="duplication">
      <consequence_terms>downstream_gene_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="lncRNA" distance="4337" gene_id="ENSG00000291178" impact="MODIFIER" strand="-1" transcript_id="ENST00000843560" variant_allele="duplication">
      <consequence_terms>downstream_gene_variant</consequence_terms>
    </transcript_consequences>
  </data>
</opt>
