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Show only entries with motif concordance for any of the selected TFs:
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Genome position
rs ID
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chr7:84824360 C>T
 rs4395839
NR2C1_HUMAN;  COT1_HUMAN;  KDM1A_HUMAN;  HDAC1_HUMAN;  HDAC2_HUMAN
K562 (myelogenous leukemia)
chr7:84824420 T>C
 rs1820962
NR2C1_HUMAN;  COT1_HUMAN;  KDM1A_HUMAN;  HDAC1_HUMAN;  NCOR1_HUMAN
K562 (myelogenous leukemia)
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