Enhancers that have rs76195798[chr14:100566527]
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Chrom. Start End Enhancer ID Tissues that enhancer appears More
chr14 100563685 100572335 enh15938
chr14 100566376 100566553 vista19090

Transcript factors that have rs76195798[chr14:100566527]
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Chrom. Start End TF name Source Predicted site? Tissue id More
chr14 100564314 100567417 ZNF143 GTRD no Epithelial (MCF-7) 108123245
chr14 100565048 100567157 ZNF143 GTRD no Epithelial (MCF-7) 108123246
chr14 100565200 100567530 ZNF274 GTRD no Cervix (HeLa-S3) 108123248
chr14 100565843 100568041 TCF7L2 GTRD no Colon (HCT116) 108123249
chr14 100565965 100569475 TCF7L2 GTRD no Colon (HCT116) 108123252
chr14 100565978 100566586 ZNF143 GTRD no Epithelial (MCF-7) 108123253
chr14 100566045 100566819 ZNF143 GTRD no Epithelial (MCF-7) 108123254
chr14 100566073 100567002 ZNF143 GTRD no Epithelial (MCF-7) 108123255
chr14 100566162 100566694 ZNF274 GTRD no Blood (GM12878) 108123256
chr14 100566339 100566758 ZNF143 GTRD no Epithelial (MCF-7) 108123257
chr14 100566374 100567487 ZNF274 GTRD no Cervix (HeLa-S3) 108123258
chr14 100566376 100567487 ZNF274 GTRD no Cervix (HeLa-S3) 108123259
chr14 100566497 100567748 TCF7L2 GTRD no Colon (HCT116) 108123260
chr14 100566527 100566541 GLIS3 JASPAR yes 107611130
chr14 100566527 100566541 GLIS3 JASPAR yes 117759058

Genes associated with rs76195798[chr14:100566527], 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