EnhancerDB
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  3. rs1558857[chr14:77470757]
Enhancers that have rs1558857[chr14:77470757]
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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 rs1558857[chr14:77470757]
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Chrom. Start End TF name Source Predicted site? Tissue id More
chr14 77469432 77470945 ZNF274 GTRD no Blood (GM12878) 21632108
chr14 77469558 77470896 ZNF274 GTRD no Blood (GM12878) 21632109
chr14 77470343 77470890 SOX2 GTRD no Neural Stem Cells (H9) 21632111
chr14 77470402 77470862 SOX2 GTRD no Neural Stem Cells (H9) 21632112
chr14 77470404 77470922 SOX2 GTRD no Neural Stem Cells (H9) 21632113
chr14 77470413 77470877 SOX2 GTRD no Neural Stem Cells (H9) 21632114
chr14 77470483 77470948 ZBTB33 GTRD no Brain (SK-N-SH) 21632116
chr14 77470504 77470831 SOX2 GTRD no Neural Stem Cells (H9) 21632117
Genes associated with rs1558857[chr14:77470757], 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