EnhancerDB
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  3. rs1861737[chr14:77480792]
Enhancers that have rs1861737[chr14:77480792]
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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 rs1861737[chr14:77480792]
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Chrom. Start End TF name Source Predicted site? Tissue id More
chr14 77480591 77480841 ZNF143 ENCODE Uniform TFBS no Embryonic Stem Cell Line (H1-hESC) 21632167
chr14 77480599 77480875 ZNF143 ENCODE Uniform TFBS no Embryonic Stem Cell Line (H1-hESC) 21632168
chr14 77480610 77480828 ZNF143 ENCODE Uniform TFBS no Embryonic Stem Cell Line (H1-hESC) 21632169
chr14 77480683 77480933 ZNF143 ENCODE Uniform TFBS no Embryonic Stem Cell Line (H1-hESC) 21632170
chr14 77480782 77480792 TEAD1 JASPAR yes 116720114
chr14 77480782 77480792 TEAD4 JASPAR yes 116720115
chr14 77480782 77480793 FOXH1 JASPAR yes 116720116
chr14 77480782 77480794 TEAD1 JASPAR yes 116720117
chr14 77480790 77480794 TEAD2 TRANSFAC yes 116720119
chr14 77480790 77480795 TBP TRANSFAC yes 116720120
Genes associated with rs1861737[chr14:77480792], 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