EnhancerDB
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  3. rs116362234[chr16:3221636]
Enhancers that have rs116362234[chr16:3221636]
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Chrom. Start End Enhancer ID Tissues that enhancer appears More
chr16 3205284 3226809 enh62538
Bone Marrow (K562) Liver (HepG2) Cervix (HeLa-S3) Brain (SK-N-MC) Prostate (RWPE1) Esophagus Colon (HCT116) Pancreas Pancreas (Panc1) Uterus Blood (T-cell) Stomach
Transcript factors that have rs116362234[chr16:3221636]
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Chrom. Start End TF name Source Predicted site? Tissue id More
chr16 3220903 3221672 TCF7L2 GTRD no Colon (HCT116) 21685655
chr16 3220903 3221672 TCF7L2 GTRD no Colon (HCT116) 108175194
chr16 3221109 3222075 ZNF143 GTRD no Epithelial (MCF-7) 108175204
chr16 3221219 3221910 ZNF274 GTRD no Bone Marrow (K562) 21685661
chr16 3221219 3221910 ZNF274 GTRD no Bone Marrow (K562) 108175205
chr16 3221237 3221779 ZNF274 GTRD no Bone Marrow (K562) 21685662
chr16 3221237 3221779 ZNF274 GTRD no Bone Marrow (K562) 108175206
chr16 3221316 3221697 ZNF274 GTRD no Liver (HepG2) 21685663
chr16 3221316 3221697 ZNF274 GTRD no Liver (HepG2) 108175209
chr16 3221395 3221751 ZNF143 ENCODE Uniform TFBS no Embryonic Stem Cell Line (H1-hESC) 108175210
chr16 3221622 3221882 ZNF274 ENCODE Uniform TFBS no Liver (HepG2) 21685665
chr16 3221630 3221639 THAP1 JASPAR yes 9208439
chr16 3221633 3221637 LFA1 TRANSFAC yes 9208440
Genes associated with rs116362234[chr16:3221636], 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