Enhancers that have rs538171011[chr14:102227248]
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Chrom. Start End Enhancer ID Tissues that enhancer appears More

Transcript factors that have rs538171011[chr14:102227248]
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Chrom. Start End TF name Source Predicted site? Tissue id More
chr14 102225768 102227963 TCF7L2 GTRD no Colon (HCT116) 108124813
chr14 102225768 102227963 TCF7L2 GTRD no Colon (HCT116) 108124814
chr14 102225863 102228022 TCF7L2 GTRD no Colon (HCT116) 108124816
chr14 102225863 102228022 TCF7L2 GTRD no Colon (HCT116) 108124817
chr14 102226439 102227312 ZNF143 GTRD no Epithelial (MCF-7) 108124828
chr14 102226439 102227312 ZNF143 GTRD no Epithelial (MCF-7) 108124829
chr14 102226707 102227929 ZNF143 GTRD no Epithelial (MCF-7) 108124842
chr14 102226707 102227929 ZNF143 GTRD no Epithelial (MCF-7) 108124843
chr14 102227065 102227435 ZNF274 ENCODE Uniform TFBS no Bone Marrow (K562) 108124855
chr14 102227165 102228033 ZNF274 GTRD no Blood (GM12878) 108124856
chr14 102227168 102227874 ZNF274 GTRD no Blood (GM12878) 108124857
chr14 102227187 102227945 ZNF143 GTRD no Epithelial (MCF-7) 108124858
chr14 102227197 102228014 ZNF143 GTRD no Epithelial (MCF-7) 108124859
chr14 102227244 102227464 ZNF274 ENCODE Uniform TFBS no Liver (HepG2) 108124860

Genes associated with rs538171011[chr14:102227248], 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