Enhancers that have rs556059626[chr14:103533675]
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Transcript factors that have rs556059626[chr14:103533675]
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Chrom. Start End TF name Source Predicted site? Tissue id More
chr14 103532309 103534664 TCF7L2 GTRD no Colon (HCT116) 21642801
chr14 103532469 103533772 TCF7L2 GTRD no Colon (HCT116) 21642803
chr14 103533043 103534486 TCF7L2 GTRD no Colon (HCT116) 21642805
chr14 103533476 103533972 ZNF217 ENCODE Uniform TFBS no Epithelial (MCF-7) 21642806
chr14 103533520 103533864 ZZZ3 ENCODE Uniform TFBS no Cervix (HeLa-S3) 21642807
chr14 103533546 103533876 ZZZ3 ENCODE Uniform TFBS no Cervix (HeLa-S3) 21642808
chr14 103533552 103533872 ZZZ3 ENCODE Uniform TFBS no Cervix (HeLa-S3) 21642809
chr14 103533559 103533889 ZZZ3 ENCODE Uniform TFBS no Cervix (HeLa-S3) 21642810
chr14 103533573 103539856 ZNF143 GTRD no Epithelial (MCF-7) 21642811
chr14 103533573 103539856 ZNF143 GTRD no Epithelial (MCF-7) 108126327
chr14 103533573 103539856 ZNF143 GTRD no Epithelial (MCF-7) 108126328
chr14 103533616 103534012 ZZZ3 ENCODE Uniform TFBS no Cervix (HeLa-S3) 21642812
chr14 103533619 103533726 ZZZ3 ENCODE Uniform TFBS no Cervix (HeLa-S3) 21642813
chr14 103533673 103533688 LEF1 JASPAR yes 117958081

Genes associated with rs556059626[chr14:103533675], 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