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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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chr10:5845207 G>A
 rs867053
PKNX1_HUMAN;  ELF1_HUMAN;  MEIS2_HUMAN;  REQU_HUMAN;  HDAC1_HUMAN...
K562 (myelogenous leukemia);  GM12878 (female B-cells)
chr10:5845220 A>G
 rs867052
IKZF1_HUMAN;  ELF1_HUMAN;  HDAC1_HUMAN;  PKNX1_HUMAN;  REQU_HUMAN...
K562 (myelogenous leukemia);  GM12878 (female B-cells)
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