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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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chr10:45261428 T>C
 rs7898089
MAFG_HUMAN;  ZN316_HUMAN;  KDM1A_HUMAN;  TAL1_HUMAN;  NCOR1_HUMAN...
K562 (myelogenous leukemia)
chr10:45261448 C>A
 rs7910028
ZN316_HUMAN;  KDM1A_HUMAN;  NCOR1_HUMAN;  MTG16_HUMAN;  SMCA4_HUMAN...
K562 (myelogenous leukemia)
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