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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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chr6:31830816 G>C
 rs565599
PEX2_HUMAN;  IKZF1_HUMAN;  ELF1_HUMAN;  NFIC_HUMAN;  ANDR_HUMAN
K562 (myelogenous leukemia);  HCT-116 (colon carcinoma);  22RV1 (prostate carcinoma)
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