EnhancerDB
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  3. rs187883927[chr13:113377655]
Enhancers that have rs187883927[chr13:113377655]
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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 rs187883927[chr13:113377655]
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Chrom. Start End TF name Source Predicted site? Tissue id More
chr13 113377161 113377691 ZZZ3 ENCODE Uniform TFBS no Cervix (HeLa-S3) 21605758
chr13 113377161 113377691 ZZZ3 ENCODE Uniform TFBS no Cervix (HeLa-S3) 108090496
chr13 113377165 113377681 ZZZ3 ENCODE Uniform TFBS no Cervix (HeLa-S3) 21605761
chr13 113377165 113377681 ZZZ3 ENCODE Uniform TFBS no Cervix (HeLa-S3) 108090499
chr13 113377218 113377674 ZZZ3 ENCODE Uniform TFBS no Cervix (HeLa-S3) 21605767
chr13 113377218 113377674 ZZZ3 ENCODE Uniform TFBS no Cervix (HeLa-S3) 108090505
chr13 113377649 113377668 PAX5 JASPAR yes 60430299
Genes associated with rs187883927[chr13:113377655], 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