Enhancers that have rs147617206[chr17:79316702]
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Chrom. Start End Enhancer ID Tissues that enhancer appears More
chr17 79309245 79326379 enh17441
chr17 79316253 79317268 vista26395

Transcript factors that have rs147617206[chr17:79316702]
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Chrom. Start End TF name Source Predicted site? Tissue id More
chr17 79315147 79316719 TCF7L2 GTRD no Colon (HCT116) 21797732
chr17 79315147 79316719 TCF7L2 GTRD no Colon (HCT116) 108308920
chr17 79315930 79316724 ZNF143 GTRD no Epithelial (MCF-7) 108308921
chr17 79316060 79316766 TCF7L2 GTRD no Colon (HCT116) 21797734
chr17 79316060 79316766 TCF7L2 GTRD no Colon (HCT116) 108308922
chr17 79316302 79316742 TCF7L2 ENCODE Uniform TFBS no Pancreas (Panc1) 108308923
chr17 79316324 79316743 TCF7L2 GTRD no Colon (HCT116) 21797735
chr17 79316324 79316743 TCF7L2 GTRD no Colon (HCT116) 108308924
chr17 79316508 79317418 ZNF143 ENCODE Uniform TFBS no Embryonic Stem Cell Line (H1-hESC) 108308926
chr17 79316533 79316877 ZNF143 ENCODE Uniform TFBS no Embryonic Stem Cell Line (H1-hESC) 108308927
chr17 79316698 79317358 ZZZ3 ENCODE Uniform TFBS no Cervix (HeLa-S3) 108308928
chr17 79316700 79316715 RFX5 JASPAR yes 21317918
chr17 79316700 79316715 RFX5 JASPAR yes 56317289

Genes associated with rs147617206[chr17:79316702], 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