EnhancerDB
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  3. rs16912192[chr11:13142197]
Enhancers that have rs16912192[chr11:13142197]
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Chrom. Start End Enhancer ID Tissues that enhancer appears More
chr11 13110005 13145006 enh28608
Bone Marrow (K562) Astrocyte Colon (HCT116) Stomach Epithelial (MCF-7) Skin (Keratinocyte) Brain (SK-N-SH) Bone (Osteoblast) Lung (A549) Peripheral Blood (MM.1S) Neural Stem Cells (H9) Thymus Prostate (PC-3) Cervix (HeLa-S3) Large Intestine Esophagus Lung (PC-9) Muscle (Myoblast) Muscle (Myotube) Liver (HepG2) Prostate (RWPE1)
Transcript factors that have rs16912192[chr11:13142197]
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Chrom. Start End TF name Source Predicted site? Tissue id More
chr11 13139516 13142231 ZNF274 GTRD no Liver (HepG2) 21472625
chr11 13139683 13142216 ZNF274 GTRD no Liver (HepG2) 21472632
chr11 13139708 13142403 ZNF274 GTRD no Liver (HepG2) 21472634
chr11 13141622 13142250 ZNF274 GTRD no Liver (HepG2) 21472718
chr11 13141853 13142369 ZZZ3 ENCODE Uniform TFBS no Cervix (HeLa-S3) 21472721
chr11 13142057 13142670 ZNF274 GTRD no Bone Marrow (K562) 21472722
chr11 13142150 13142654 ZZZ3 ENCODE Uniform TFBS no Cervix (HeLa-S3) 21472723
chr11 13142185 13142200 FOXP1 JASPAR yes 37506572
chr11 13142186 13142199 POU2F2 JASPAR yes 37506573
Genes associated with rs16912192[chr11:13142197], 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