EnhancerDB
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  3. rs4899632[chr14:77467129]
Enhancers that have rs4899632[chr14:77467129]
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Chrom. Start End Enhancer ID Tissues that enhancer appears More
chr14 77458104 77493935 enh3336
Colon (HCT116) Blood (Karpas-422) Embryonic Stem Cell Line (H1-hESC) Pancreas Uterus Blood (T-cell) Epithelial (MCF-7) Stomach Skin (Keratinocyte) Brain (SK-N-SH) Bone (Osteoblast) Thyroid Peripheral Blood (MM.1S) Neural Stem Cells (H9) Thymus Prostate (PC-3) Cervix (HeLa-S3) Large Intestine Esophagus Blood (GM12878) Placenta Lung (PC-9) Prostate (RWPE1) Muscle (A673) Heart
chr14 77466876 77467234 vista18548
VISTA
Transcript factors that have rs4899632[chr14:77467129]
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Chrom. Start End TF name Source Predicted site? Tissue id More
chr14 77466840 77467170 ZZZ3 ENCODE Uniform TFBS no Blood (GM12878) 21632090
chr14 77466840 77467170 ZZZ3 ENCODE Uniform TFBS no Blood (GM12878) 108115383
chr14 77466849 77467159 ZNF274 ENCODE Uniform TFBS no Bone Marrow (K562) 108115384
chr14 77466951 77467315 ZZZ3 ENCODE Uniform TFBS no Blood (GM12878) 21632091
chr14 77466951 77467315 ZZZ3 ENCODE Uniform TFBS no Blood (GM12878) 108115385
chr14 77467123 77467143 TP63 JASPAR yes 107586512
chr14 77467123 77467143 TP63 JASPAR yes 116718187
chr14 77467125 77467140 TP53 JASPAR yes 107586513
chr14 77467125 77467140 TP53 JASPAR yes 116718188
chr14 77467125 77467145 TP53 JASPAR yes 107586514
chr14 77467125 77467145 TP53 JASPAR yes 116718189
Genes associated with rs4899632[chr14:77467129], 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