EnhancerDB
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  3. rs551613792[chr16:81667096]
Enhancers that have rs551613792[chr16:81667096]
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Chrom. Start End Enhancer ID Tissues that enhancer appears More
chr16 81653149 81684095 enh16840
Bone Marrow (K562) Astrocyte Colon (HCT116) Embryonic Stem Cell Line (H1-hESC) Pancreas Blood (T-cell) Kidney Epithelial (MCF-7) Stomach Ovary Bone (Osteoblast) Thyroid Peripheral Blood (MM.1S) Neural Stem Cells (H9) Thymus Prostate (PC-3) Large Intestine Esophagus Placenta Lung (PC-9) Breast Muscle (Myoblast) Liver (HepG2) Prostate (RWPE1)
Transcript factors that have rs551613792[chr16:81667096]
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Chrom. Start End TF name Source Predicted site? Tissue id More
chr16 81666359 81667116 ZNF274 GTRD no Blood (GM12878) 108209882
chr16 81666380 81667193 ZNF274 GTRD no Blood (GM12878) 108209883
chr16 81666491 81667214 TCF7L2 GTRD no Colon (HCT116) 21717719
chr16 81666491 81667214 TCF7L2 GTRD no Colon (HCT116) 108209893
chr16 81666753 81667197 CTCF UCSC Txn Factor no Conserved 108209905
chr16 81666813 81667103 ZNF143 ENCODE Uniform TFBS no Embryonic Stem Cell Line (H1-hESC) 21717729
chr16 81666813 81667103 ZNF143 ENCODE Uniform TFBS no Embryonic Stem Cell Line (H1-hESC) 108209907
chr16 81666834 81667561 ZNF274 GTRD no Liver (HepG2) 21717731
chr16 81666834 81667561 ZNF274 GTRD no Liver (HepG2) 108209909
Genes associated with rs551613792[chr16:81667096], 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