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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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chr5:31532771 C>A
 rs10070102
MNT_HUMAN;  MGAP_HUMAN;  EP400_HUMAN;  HDAC1_HUMAN;  MXI1_HUMAN...
K562 (myelogenous leukemia)
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