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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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chr4:190110342 A>G
 rs71256047
ZFX_HUMAN;  CEBPG_HUMAN;  CTCF_HUMAN
K562 (myelogenous leukemia);  GM12878 (female B-cells lymphoblastoid cell line);  HepG2 (hepatoblastoma)...
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