Enhancers that have rs188512786[chr17:79700756]
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Transcript factors that have rs188512786[chr17:79700756]
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Chrom. Start End TF name Source Predicted site? Tissue id More
chr17 79697872 79702757 TCF7L2 GTRD no Colon (HCT116) 21798308
chr17 79697872 79702757 TCF7L2 GTRD no Colon (HCT116) 108310128
chr17 79698203 79702705 TCF7L2 GTRD no Colon (HCT116) 21798310
chr17 79698203 79702705 TCF7L2 GTRD no Colon (HCT116) 108310134
chr17 79698423 79701576 TCF7L2 GTRD no Colon (HCT116) 21798312
chr17 79698423 79701576 TCF7L2 GTRD no Colon (HCT116) 108310138
chr17 79698493 79701154 TCF7L2 GTRD no Colon (HCT116) 21798314
chr17 79698680 79700810 TCF7L2 GTRD no Colon (HCT116) 21798315
chr17 79698846 79701373 TCF7L2 GTRD no Colon (HCT116) 21798317
chr17 79698921 79702115 TCF7L2 GTRD no Colon (HCT116) 21798320
chr17 79700212 79700944 TCF7L2 GTRD no Colon (HCT116) 21798326
chr17 79700337 79701127 ZNF274 ENCODE Uniform TFBS no Liver (HepG2) 21798327
chr17 79700577 79701319 ZNF143 GTRD no Epithelial (MCF-7) 21798328
chr17 79700669 79701011 ZNF274 GTRD no Cervix (HeLa-S3) 21798329
chr17 79700689 79701153 ZBTB33 ENCODE Uniform TFBS no Colon (HCT116) 21798330
chr17 79700693 79701157 ZZZ3 ENCODE Uniform TFBS no Cervix (HeLa-S3) 21798331
chr17 79700731 79701067 ZNF274 ENCODE Uniform TFBS no Liver (HepG2) 21798332
chr17 79700741 79700756 TFAP2C JASPAR yes 56340726

Genes associated with rs188512786[chr17:79700756], comfirmed by eQTL
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Blank TSI value indicates lack of sufficient expression for calculation
Chrom. Start End Strand Gene name Ensembl ID TSS of gene Distance between TSS and SNP Tissue q Value id More