EnhancerDB
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  3. rs184037159[chr14:77485552]
Enhancers that have rs184037159[chr14:77485552]
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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 rs184037159[chr14:77485552]
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Chrom. Start End TF name Source Predicted site? Tissue id More
chr14 77485132 77486048 ZNF143 GTRD no Epithelial (MCF-7) 21632179
chr14 77485150 77485998 ZNF143 GTRD no Epithelial (MCF-7) 21632180
chr14 77485195 77485905 ZNF143 GTRD no Epithelial (MCF-7) 21632181
chr14 77485200 77485888 ZNF143 GTRD no Epithelial (MCF-7) 21632182
chr14 77485215 77485908 ZNF143 GTRD no Epithelial (MCF-7) 21632183
chr14 77485235 77485939 TCF7L2 GTRD no Colon (HCT116) 21632184
chr14 77485239 77485831 ZNF143 GTRD no Epithelial (MCF-7) 21632185
chr14 77485259 77485962 ZNF143 GTRD no Epithelial (MCF-7) 21632186
chr14 77485312 77485887 ZNF143 GTRD no Epithelial (MCF-7) 21632187
Genes associated with rs184037159[chr14:77485552], 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