EnhancerDB
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  3. rs4907751[chr13:113394650]
Enhancers that have rs4907751[chr13:113394650]
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Chrom. Start End Enhancer ID Tissues that enhancer appears More
chr13 113356925 113401095 enh15512
Bone Marrow (K562) Brain (SK-N-MC) Astrocyte Colon (HCT116) Embryonic Stem Cell Line (H1-hESC) Pancreas Uterus Epithelial (MCF-7) Stomach Skin (Keratinocyte) Brain (SK-N-SH) Ovary Bone (Osteoblast) Thyroid Neural Stem Cells (H9) Thymus Prostate (PC-3) Cervix (HeLa-S3) Large Intestine Esophagus Placenta Lung (PC-9) Muscle (Myoblast) Spleen Muscle (Myotube) Liver (HepG2) Prostate (RWPE1) Lung Heart
Transcript factors that have rs4907751[chr13:113394650]
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Chrom. Start End TF name Source Predicted site? Tissue id More
chr13 113392878 113394948 ZNF274 GTRD no Cervix (HeLa-S3) 21605781
chr13 113392878 113394948 ZNF274 GTRD no Cervix (HeLa-S3) 108090521
chr13 113393046 113394829 ZNF143 GTRD no Epithelial (MCF-7) 21605783
chr13 113393046 113394829 ZNF143 GTRD no Epithelial (MCF-7) 108090523
chr13 113393151 113394737 ZNF274 GTRD no Blood (GM12878) 108090524
chr13 113394636 113394656 RREB1 JASPAR yes 60432866
chr13 113394648 113394663 MEF2A JASPAR yes 60432867
chr13 113394649 113394664 MEF2C JASPAR yes 60432868
Genes associated with rs4907751[chr13:113394650], 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