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Show only entries with motif concordance for any of the selected TFs:
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Genome position
rs ID
Top 5 TFs
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chr18:48963995 C>T
 rs72919622
PKNX1_HUMAN;  MEIS2_HUMAN;  IKZF1_HUMAN;  ARI1B_HUMAN;  PBX2_HUMAN
K562 (myelogenous leukemia)
chr18:48964027 G>T
 rs7240835
PKNX1_HUMAN;  IKZF1_HUMAN;  MEIS2_HUMAN;  ARI1B_HUMAN;  PBX2_HUMAN
K562 (myelogenous leukemia)
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