EnhancerDB
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  3. rs139496292[chr16:1327470]
Enhancers that have rs139496292[chr16:1327470]
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Chrom. Start End Enhancer ID Tissues that enhancer appears More
chr16 1326605 1349655 enh16494
Astrocyte Colon (HCT116) Pancreas Stomach Epithelial (MCF-7) Skin (Keratinocyte) Blood (OCI-LY7) Thyroid Peripheral Blood (MM.1S) Pancreas (Panc1) Prostate (PC-3) Cervix (HeLa-S3) Large Intestine Esophagus Placenta Lung (PC-9) Muscle (Myoblast) Muscle (Myotube) Liver (HepG2) Prostate (RWPE1) Muscle (A673)
Transcript factors that have rs139496292[chr16:1327470]
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Chrom. Start End TF name Source Predicted site? Tissue id More
chr16 1326734 1327890 TCF7L2 GTRD no Colon (HCT116) 21684396
chr16 1326907 1328478 TCF7L2 GTRD no Colon (HCT116) 21684397
chr16 1326924 1327655 TCF7L2 GTRD no Colon (HCT116) 21684398
chr16 1326958 1327818 ZNF274 GTRD no Liver (HepG2) 21684399
chr16 1326969 1328022 TCF7L2 GTRD no Colon (HCT116) 21684400
chr16 1326971 1327632 TCF7L2 GTRD no Colon (HCT116) 21684401
chr16 1326981 1328229 ZNF143 GTRD no Epithelial (MCF-7) 21684402
chr16 1326998 1328199 TCF7L2 GTRD no Colon (HCT116) 21684403
chr16 1327355 1328228 ZNF143 GTRD no Epithelial (MCF-7) 21684404
chr16 1327420 1328210 ZNF274 ENCODE Uniform TFBS no Liver (HepG2) 21684405
Genes associated with rs139496292[chr16:1327470], 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