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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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Top 3 cell types
chr19:12441249 G>C
 rs3745655
PBX1_HUMAN;  RBM25_HUMAN;  CTCF_HUMAN;  FOXA2_HUMAN;  BCL6_HUMAN
ICN12 (primary pre-B acute lymphomablastic leukemia);  2588 (Lymphoblastoid Cell Lines);  HepG2 (hepatoblastoma)
chr19:12441288 T>G
 rs59876891
ICN12 (primary pre-B acute lymphomablastic leukemia);  2588 (Lymphoblastoid Cell Lines)
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