<opt>
  <data id="9_22125503_-/C" allele_string="-/C" assembly_name="GRCh37" end="22125502" input="9 22125503 22125502 -/C 1" most_severe_consequence="downstream_gene_variant" seq_region_name="9" start="22125503" strand="1">
    <transcript_consequences biotype="antisense" distance="4406" gene_id="ENSG00000240498" gene_symbol="CDKN2B-AS1" gene_symbol_source="HGNC" hgnc_id="34341" impact="MODIFIER" strand="1" transcript_id="ENST00000422420" variant_allele="C">
      <consequence_terms>downstream_gene_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="antisense" distance="4408" gene_id="ENSG00000240498" gene_symbol="CDKN2B-AS1" gene_symbol_source="HGNC" hgnc_id="34341" impact="MODIFIER" strand="1" transcript_id="ENST00000428597" variant_allele="C">
      <consequence_terms>downstream_gene_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="antisense" distance="4931" gene_id="ENSG00000240498" gene_symbol="CDKN2B-AS1" gene_symbol_source="HGNC" hgnc_id="34341" impact="MODIFIER" strand="1" transcript_id="ENST00000577551" variant_allele="C">
      <consequence_terms>downstream_gene_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="antisense" distance="4857" gene_id="ENSG00000240498" gene_symbol="CDKN2B-AS1" gene_symbol_source="HGNC" hgnc_id="34341" impact="MODIFIER" strand="1" transcript_id="ENST00000580576" variant_allele="C">
      <consequence_terms>downstream_gene_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="antisense" distance="4931" gene_id="ENSG00000240498" gene_symbol="CDKN2B-AS1" gene_symbol_source="HGNC" hgnc_id="34341" impact="MODIFIER" strand="1" transcript_id="ENST00000581051" variant_allele="C">
      <consequence_terms>downstream_gene_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="antisense" distance="4931" gene_id="ENSG00000240498" gene_symbol="CDKN2B-AS1" gene_symbol_source="HGNC" hgnc_id="34341" impact="MODIFIER" strand="1" transcript_id="ENST00000582072" variant_allele="C">
      <consequence_terms>downstream_gene_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="antisense" distance="4931" gene_id="ENSG00000240498" gene_symbol="CDKN2B-AS1" gene_symbol_source="HGNC" hgnc_id="34341" impact="MODIFIER" strand="1" transcript_id="ENST00000584020" variant_allele="C">
      <consequence_terms>downstream_gene_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="antisense" distance="4931" gene_id="ENSG00000240498" gene_symbol="CDKN2B-AS1" gene_symbol_source="HGNC" hgnc_id="34341" impact="MODIFIER" strand="1" transcript_id="ENST00000584637" variant_allele="C">
      <consequence_terms>downstream_gene_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="antisense" distance="4931" gene_id="ENSG00000240498" gene_symbol="CDKN2B-AS1" gene_symbol_source="HGNC" hgnc_id="34341" impact="MODIFIER" strand="1" transcript_id="ENST00000584816" variant_allele="C">
      <consequence_terms>downstream_gene_variant</consequence_terms>
    </transcript_consequences>
    <transcript_consequences biotype="antisense" distance="4959" gene_id="ENSG00000240498" gene_symbol="CDKN2B-AS1" gene_symbol_source="HGNC" hgnc_id="34341" impact="MODIFIER" strand="1" transcript_id="ENST00000585267" variant_allele="C">
      <consequence_terms>downstream_gene_variant</consequence_terms>
    </transcript_consequences>
  </data>
</opt>
