<opt>
  <data id="7_100318423_duplication" allele_string="duplication" assembly_name="GRCh37" end="100321323" input="7 100318423 100321323 DUP 1" most_severe_consequence="transcript_amplification" seq_region_name="7" start="100318423" strand="1">
    <motif_feature_consequences bp_overlap="16" impact="MODIFIER" motif_feature_id="ELK1_HOXB13_AAD_TCTATG40NTAG_RNCGGAANYNRTWAAN_m1_c2" percentage_overlap="100" variant_allele="duplication">
      <consequence_terms>TFBS_amplification</consequence_terms>
      <consequence_terms>TF_binding_site_variant</consequence_terms>
    </motif_feature_consequences>
    <motif_feature_consequences bp_overlap="13" impact="MODIFIER" motif_feature_id="ERF_FOXI1_AAC_TAGTCA40NTCT_TGTTKMCGGAWRN_m1_c2" percentage_overlap="100" variant_allele="duplication">
      <consequence_terms>TFBS_amplification</consequence_terms>
      <consequence_terms>TF_binding_site_variant</consequence_terms>
    </motif_feature_consequences>
    <motif_feature_consequences bp_overlap="16" impact="MODIFIER" motif_feature_id="ERF_HOXB13_AAC_TGCGAC40NGGT_NNMGGAARNNRTAAAN_m1_c2" percentage_overlap="100" variant_allele="duplication">
      <consequence_terms>TFBS_amplification</consequence_terms>
      <consequence_terms>TF_binding_site_variant</consequence_terms>
    </motif_feature_consequences>
    <motif_feature_consequences bp_overlap="14" impact="MODIFIER" motif_feature_id="ETV2_HOXA2_AAA_TTAACA40NTGT_NCCGGAAGTMATTA_m2_c3" percentage_overlap="100" variant_allele="duplication">
      <consequence_terms>TFBS_amplification</consequence_terms>
      <consequence_terms>TF_binding_site_variant</consequence_terms>
    </motif_feature_consequences>
    <motif_feature_consequences bp_overlap="11" impact="MODIFIER" motif_feature_id="ETV5_EVX1_AY_TCGTGA40NGTC_RSCGGWAATKR_m1_c3" percentage_overlap="100" variant_allele="duplication">
      <consequence_terms>TFBS_amplification</consequence_terms>
      <consequence_terms>TF_binding_site_variant</consequence_terms>
    </motif_feature_consequences>
    <motif_feature_consequences bp_overlap="14" impact="MODIFIER" motif_feature_id="FOXO1_ELF1_AS_TTTCAC40NGTG_RWMAACAGGAAGTN_m1_c2" percentage_overlap="100" variant_allele="duplication">
      <consequence_terms>TFBS_amplification</consequence_terms>
      <consequence_terms>TF_binding_site_variant</consequence_terms>
    </motif_feature_consequences>
    <motif_feature_consequences bp_overlap="13" impact="MODIFIER" motif_feature_id="FOXO1_ELK1_AS_TTCGCT40NCTT_RSCGGATGTTRTN_m1_c2" percentage_overlap="100" variant_allele="duplication">
      <consequence_terms>TFBS_amplification</consequence_terms>
      <consequence_terms>TF_binding_site_variant</consequence_terms>
    </motif_feature_consequences>
    <motif_feature_consequences bp_overlap="15" impact="MODIFIER" motif_feature_id="GCM1_ELK1_AU_TTCGCT40NCTT_RTGCGGGCGGAAGTN_m1_c3" percentage_overlap="100" variant_allele="duplication">
      <consequence_terms>TFBS_amplification</consequence_terms>
      <consequence_terms>TF_binding_site_variant</consequence_terms>
    </motif_feature_consequences>
    <motif_feature_consequences bp_overlap="15" impact="MODIFIER" motif_feature_id="GCM1_ELK3_AU_TTGGGT40NGGC_RTGCGGGCGGAAGTN_m2_c3" percentage_overlap="100" variant_allele="duplication">
      <consequence_terms>TFBS_amplification</consequence_terms>
      <consequence_terms>TF_binding_site_variant</consequence_terms>
    </motif_feature_consequences>
    <motif_feature_consequences bp_overlap="17" impact="MODIFIER" motif_feature_id="HOXD12_ELK1_AAB_TTCGCT40NCTT_NRSCGGAAGNNGTAAAN_m1_c2" percentage_overlap="100" variant_allele="duplication">
      <consequence_terms>TFBS_amplification</consequence_terms>
      <consequence_terms>TF_binding_site_variant</consequence_terms>
    </motif_feature_consequences>
    <motif_feature_consequences bp_overlap="13" impact="MODIFIER" motif_feature_id="POU2F1_ETV1_AS_TGCGAA40NAGC_NCCGGATATGCAN_m1_c2u" percentage_overlap="100" variant_allele="duplication">
      <consequence_terms>TFBS_amplification</consequence_terms>
      <consequence_terms>TF_binding_site_variant</consequence_terms>
    </motif_feature_consequences>
    <motif_feature_consequences bp_overlap="14" impact="MODIFIER" motif_feature_id="TEAD4_ELF1_AY_TGTGAG40NAGG_GGAATGCGGAAGTN_m2_c2" percentage_overlap="100" variant_allele="duplication">
      <consequence_terms>TFBS_amplification</consequence_terms>
      <consequence_terms>TF_binding_site_variant</consequence_terms>
    </motif_feature_consequences>
    <motif_feature_consequences bp_overlap="10" impact="MODIFIER" motif_feature_id="GABPA_AG_TGGCCC20NCCT_ACCGGAAGTN_m1_c4_Cell2013" percentage_overlap="100" variant_allele="duplication">
      <consequence_terms>TFBS_amplification</consequence_terms>
      <consequence_terms>TF_binding_site_variant</consequence_terms>
    </motif_feature_consequences>
    <regulatory_feature_consequences bp_overlap="379" impact="MODIFIER" percentage_overlap="47.26" regulatory_feature_id="ENSR00001404926" variant_allele="duplication">
      <consequence_terms>regulatory_region_variant</consequence_terms>
    </regulatory_feature_consequences>
    <transcript_consequences biotype="protein_coding" bp_overlap="2901" gene_id="ENSG00000130427" gene_symbol="EPO" gene_symbol_source="HGNC" hgnc_id="3415" impact="HIGH" percentage_overlap="100" strand="1" transcript_id="ENST00000252723" variant_allele="duplication">
      <consequence_terms>transcript_amplification</consequence_terms>
    </transcript_consequences>
  </data>
</opt>
