EnhancerDB
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  3. rs11646668[chr16:73066954]
Enhancers that have rs11646668[chr16:73066954]
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Chrom. Start End Enhancer ID Tissues that enhancer appears More
chr16 73046817 73092190 enh16770
Bone Marrow (K562) Astrocyte Colon (HCT116) Adrenal Pancreas Uterus Epithelial (MCF-7) Stomach Brain (SK-N-SH) Bone (Osteoblast) Blood (OCI-LY7) Thyroid Peripheral Blood (MM.1S) Pancreas (Panc1) Prostate (PC-3) Cervix (HeLa-S3) Large Intestine Esophagus Blood (GM12878) Placenta Lung (PC-9) Breast Muscle (Myoblast) Muscle (Myotube) Liver (HepG2) Prostate (RWPE1) Muscle (A673) Heart
Transcript factors that have rs11646668[chr16:73066954]
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Chrom. Start End TF name Source Predicted site? Tissue id More
chr16 73065883 73067739 ZNF143 GTRD no Epithelial (MCF-7) 21714112
chr16 73065883 73067739 ZNF143 GTRD no Epithelial (MCF-7) 108205786
chr16 73065893 73067589 TCF7L2 GTRD no Colon (HCT116) 21714113
chr16 73065893 73067589 TCF7L2 GTRD no Colon (HCT116) 108205787
chr16 73066639 73071091 ZNF274 GTRD no Cervix (HeLa-S3) 21714114
chr16 73066639 73071091 ZNF274 GTRD no Cervix (HeLa-S3) 108205788
chr16 73066776 73067559 SOX2 GTRD no Neural Stem Cells (H9) 108205789
chr16 73066836 73067446 ZNF143 ENCODE Uniform TFBS no Embryonic Stem Cell Line (H1-hESC) 108205790
chr16 73066931 73067584 TCF7L2 GTRD no Colon (HCT116) 21714115
chr16 73066931 73067584 TCF7L2 GTRD no Colon (HCT116) 108205791
Genes associated with rs11646668[chr16:73066954], 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