EnhancerDB
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Enhancers that have rs179138[chr14:95990728]
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Chrom. Start End Enhancer ID Tissues that enhancer appears More
chr14 95980405 95994595 enh15901
Brain (SK-N-MC) Liver Astrocyte Colon (HCT116) Uterus Blood (T-cell) Epithelial (MCF-7) Stomach Skin (Keratinocyte) Bone (Osteoblast) Blood (OCI-LY7) Thymus Prostate (PC-3) Cervix (HeLa-S3) Esophagus Placenta Lung (PC-9) Liver (HepG2) Prostate (RWPE1) Muscle (A673) Heart
Transcript factors that have rs179138[chr14:95990728]
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Chrom. Start End TF name Source Predicted site? Tissue id More
chr14 95989518 95990913 ZNF143 GTRD no Epithelial (MCF-7) 21636764
chr14 95990436 95990912 ZZZ3 ENCODE Uniform TFBS no Cervix (HeLa-S3) 21636788
chr14 95990448 95990764 ZNF274 ENCODE Uniform TFBS no Liver (HepG2) 21636789
chr14 95990481 95990817 ZNF274 ENCODE Uniform TFBS no Liver (HepG2) 21636790
chr14 95990492 95990782 ZNF274 ENCODE Uniform TFBS no Liver (HepG2) 21636791
chr14 95990556 95990846 ZBTB33 ENCODE Uniform TFBS no Colon (HCT116) 21636792
chr14 95990582 95990779 ZNF274 ENCODE Uniform TFBS no Liver (HepG2) 21636793
chr14 95990593 95990783 ZNF217 ENCODE Uniform TFBS no Epithelial (MCF-7) 21636794
chr14 95990605 95990835 ZNF274 ENCODE Uniform TFBS no Liver (HepG2) 21636795
Genes associated with rs179138[chr14:95990728], 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