Enhancers that have rs115010482[chr14:75697478]
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Transcript factors that have rs115010482[chr14:75697478]
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Chrom. Start End TF name Source Predicted site? Tissue id More
chr14 75697072 75697722 ZZZ3 ENCODE Uniform TFBS no Cervix (HeLa-S3) 21629718
chr14 75697072 75697722 ZZZ3 ENCODE Uniform TFBS no Cervix (HeLa-S3) 108113890
chr14 75697142 75697646 ZZZ3 ENCODE Uniform TFBS no Cervix (HeLa-S3) 21629720
chr14 75697142 75697646 ZZZ3 ENCODE Uniform TFBS no Cervix (HeLa-S3) 108113892
chr14 75697180 75697696 ZZZ3 ENCODE Uniform TFBS no Cervix (HeLa-S3) 21629721
chr14 75697180 75697696 ZZZ3 ENCODE Uniform TFBS no Cervix (HeLa-S3) 108113893
chr14 75697229 75697519 ZBTB33 ENCODE Uniform TFBS no Colon (HCT116) 21629724
chr14 75697229 75697519 ZBTB33 ENCODE Uniform TFBS no Colon (HCT116) 108113896
chr14 75697263 75697493 ZZZ3 ENCODE Uniform TFBS no Cervix (HeLa-S3) 21629725
chr14 75697263 75697493 ZZZ3 ENCODE Uniform TFBS no Cervix (HeLa-S3) 108113897
chr14 75697324 75697660 POL24H8 ENCODE Uniform TFBS no Brain (SK-N-MC) 21629726
chr14 75697324 75697660 POL24H8 ENCODE Uniform TFBS no Brain (SK-N-MC) 108113898
chr14 75697468 75697483 HNF4A JASPAR yes 116611242
chr14 75697469 75697484 HNF4G JASPAR yes 116611243

Genes associated with rs115010482[chr14:75697478], 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