EnhancerDB
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  3. rs551581162[chr14:77492381]
Enhancers that have rs551581162[chr14:77492381]
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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
Transcript factors that have rs551581162[chr14:77492381]
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Chrom. Start End TF name Source Predicted site? Tissue id More
chr14 77491872 77492488 ZNF143 ENCODE Uniform TFBS no Embryonic Stem Cell Line (H1-hESC) 21632238
chr14 77491990 77492590 ZNF143 ENCODE Uniform TFBS no Embryonic Stem Cell Line (H1-hESC) 21632240
chr14 77492265 77492901 ZNF143 ENCODE Uniform TFBS no Embryonic Stem Cell Line (H1-hESC) 21632244
chr14 77492329 77492519 ZNF217 ENCODE Uniform TFBS no Epithelial (MCF-7) 21632245
chr14 77492379 77492390 TFAP2A JASPAR yes 116721864
chr14 77492379 77492390 TFAP2B JASPAR yes 116721865
chr14 77492379 77492390 TFAP2C JASPAR yes 116721866
chr14 77492380 77492389 TFAP2A JASPAR yes 116721867
Genes associated with rs551581162[chr14:77492381], 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