EnhancerDB
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  3. rs180842096[chr14:77403785]
Enhancers that have rs180842096[chr14:77403785]
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Chrom. Start End Enhancer ID Tissues that enhancer appears More
chr14 77400862 77447355 enh3335
Bone Marrow (K562) Brain (SK-N-MC) Liver Astrocyte Colon (HCT116) Adrenal Blood (Karpas-422) Embryonic Stem Cell Line (H1-hESC) Pancreas Uterus Blood (T-cell) Epithelial (MCF-7) Kidney Skin (Keratinocyte) Stomach Brain (SK-N-SH) Ovary Bone (Osteoblast) Thyroid Peripheral Blood (MM.1S) Pancreas (Panc1) Neural Stem Cells (H9) Thymus Prostate (PC-3) Cervix (HeLa-S3) Large Intestine Esophagus Blood (GM12878) Placenta Lung (PC-9) Breast Muscle (Myoblast) Spleen Muscle (Myotube) Liver (HepG2) Prostate (RWPE1) Lung Muscle (A673) Heart
chr14 77402795 77405507 vista478
VISTA
Transcript factors that have rs180842096[chr14:77403785]
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Chrom. Start End TF name Source Predicted site? Tissue id More
chr14 77403487 77404007 ZNF143 ENCODE Uniform TFBS no Embryonic Stem Cell Line (H1-hESC) 21631141
chr14 77403487 77404007 ZNF143 ENCODE Uniform TFBS no Embryonic Stem Cell Line (H1-hESC) 107686734
chr14 77403604 77403900 POL24H8 ENCODE Uniform TFBS no Brain (SK-N-MC) 21631142
chr14 77403770 77404248 ZNF274 GTRD no Bone Marrow (K562) 21631143
Genes associated with rs180842096[chr14:77403785], 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