EnhancerDB
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Enhancers that have rs55663734[chr14:93510695]
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Chrom. Start End Enhancer ID Tissues that enhancer appears More
chr14 93466938 93531515 enh15884
Bone Marrow (K562) Brain (SK-N-MC) Astrocyte Colon (HCT116) Embryonic Stem Cell Line (H1-hESC) Pancreas Uterus Blood (T-cell) Epithelial (MCF-7) Stomach Brain (SK-N-SH) Bone (Osteoblast) Thyroid Neural Stem Cells (H9) Thymus Prostate (PC-3) Cervix (HeLa-S3) Large Intestine Esophagus Blood (GM12878) Placenta Lung (PC-9) Breast Muscle (Myoblast) Muscle (Myotube) Liver (HepG2) Prostate (RWPE1) Muscle (A673) Heart
chr14 93510584 93510744 vista18880
VISTA
Transcript factors that have rs55663734[chr14:93510695]
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Chrom. Start End TF name Source Predicted site? Tissue id More
chr14 93510503 93510899 ZZZ3 ENCODE Uniform TFBS no Cervix (HeLa-S3) 21635314
chr14 93510503 93510899 ZZZ3 ENCODE Uniform TFBS no Cervix (HeLa-S3) 108120322
chr14 93510515 93510779 ZZZ3 ENCODE Uniform TFBS no Cervix (HeLa-S3) 21635315
chr14 93510515 93510779 ZZZ3 ENCODE Uniform TFBS no Cervix (HeLa-S3) 108120323
chr14 93510516 93510836 ZZZ3 ENCODE Uniform TFBS no Cervix (HeLa-S3) 21635316
chr14 93510516 93510836 ZZZ3 ENCODE Uniform TFBS no Cervix (HeLa-S3) 108120324
Genes associated with rs55663734[chr14:93510695], 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