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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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chr2:69182090 C>T
 rs6752908
ARI1B_HUMAN;  ATF3_HUMAN;  MTG16_HUMAN;  NCOR1_HUMAN;  NRF1_HUMAN...
K562 (myelogenous leukemia)
chr2:69182133 A>G
 rs6724204
ARI1B_HUMAN;  ATF3_HUMAN;  MTG16_HUMAN;  NRF1_HUMAN;  NCOR1_HUMAN...
K562 (myelogenous leukemia)
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