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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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chr17:56834568 G>A
 rs2235092
ZBT26_HUMAN;  RING2_HUMAN;  KDM1A_HUMAN;  NFIC_HUMAN;  SP2_HUMAN
K562 (myelogenous leukemia);  HEK293 (embryonic kidney);  GM12878 (female B-cells)
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