Enhancers that have rs764432[chr17:6478489]
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Chrom. Start End Enhancer ID Tissues that enhancer appears More
chr17 6476411 6481071 enh32069

Transcript factors that have rs764432[chr17:6478489]
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Chrom. Start End TF name Source Predicted site? Tissue id More
chr17 6477830 6478969 TCF7L2 GTRD no Colon (HCT116) 108233394
chr17 6477881 6478999 TCF7L2 GTRD no Colon (HCT116) 108233395
chr17 6478336 6479366 ZNF274 GTRD no Cervix (HeLa-S3) 108233396
chr17 6478348 6478799 TCF7L2 GTRD no Colon (HCT116) 108233397
chr17 6478422 6479082 ZZZ3 ENCODE Uniform TFBS no Blood (GM12878) 108233398
chr17 6478427 6478922 ZNF143 GTRD no Epithelial (MCF-7) 108233399
chr17 6478427 6479062 ZNF143 GTRD no Epithelial (MCF-7) 108233400
chr17 6478433 6478987 TCF7L2 GTRD no Colon (HCT116) 108233401
chr17 6478440 6478906 ZNF143 GTRD no Epithelial (MCF-7) 108233402
chr17 6478455 6478765 ZNF274 ENCODE Uniform TFBS no Bone Marrow (K562) 21740830
chr17 6478455 6478765 ZNF274 ENCODE Uniform TFBS no Bone Marrow (K562) 108233403
chr17 6478467 6478737 ZNF143 ENCODE Uniform TFBS no Embryonic Stem Cell Line (H1-hESC) 108233404
chr17 6478471 6478721 ZNF143 ENCODE Uniform TFBS no Embryonic Stem Cell Line (H1-hESC) 108233405
chr17 6478480 6479110 ZZZ3 ENCODE Uniform TFBS no Blood (GM12878) 108233406

Genes associated with rs764432[chr17:6478489], 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