EnhancerDB
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  3. rs111641569[chr11:61768717]
Enhancers that have rs111641569[chr11:61768717]
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Chrom. Start End Enhancer ID Tissues that enhancer appears More
chr11 61760605 61775094 enh43550
Liver (HepG2) Brain (SK-N-MC) Large Intestine Ovary Bone (Osteoblast) Colon (HCT116) Uterus Muscle (Myoblast) Pancreas Muscle (Myotube) Neural Stem Cells (H9) Stomach
Transcript factors that have rs111641569[chr11:61768717]
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Chrom. Start End TF name Source Predicted site? Tissue id More
chr11 61768022 61770262 ZNF274 GTRD no Liver (HepG2) 21487449
chr11 61768402 61770298 ZNF274 GTRD no Liver (HepG2) 21487458
chr11 61768468 61770192 ZNF274 GTRD no Liver (HepG2) 21487459
chr11 61768471 61769196 ZNF274 GTRD no Liver (HepG2) 21487460
chr11 61768491 61769958 TCF7L2 GTRD no Colon (HCT116) 21487461
chr11 61768492 61768892 ZNF274 ENCODE Uniform TFBS no Liver (HepG2) 21487462
chr11 61768553 61769150 ZNF274 GTRD no Liver (HepG2) 21487463
chr11 61768563 61770121 ZNF274 GTRD no Liver (HepG2) 21487464
chr11 61768577 61769234 ZNF274 GTRD no Liver (HepG2) 21487465
chr11 61768630 61770650 ZNF274 GTRD no Liver (HepG2) 21487466
chr11 61768632 61769992 ZNF274 GTRD no Liver (HepG2) 21487467
chr11 61768648 61770071 ZNF274 GTRD no Liver (HepG2) 21487468
chr11 61768666 61770859 TCF7L2 GTRD no Colon (HCT116) 21487469
Genes associated with rs111641569[chr11:61768717], 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