Enhancers that have rs534946298[chr14:95981464]
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Transcript factors that have rs534946298[chr14:95981464]
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Chrom. Start End TF name Source Predicted site? Tissue id More
chr14 95981237 95981643 SOX2 GTRD no Neural Stem Cells (H9) 108121479
chr14 95981237 95981643 SOX2 GTRD no Neural Stem Cells (H9) 108121480
chr14 95981246 95981590 SOX2 GTRD no Neural Stem Cells (H9) 108121482
chr14 95981246 95981590 SOX2 GTRD no Neural Stem Cells (H9) 108121483
chr14 95981267 95981878 TCF7L2 GTRD no Colon (HCT116) 21636731
chr14 95981267 95981878 TCF7L2 GTRD no Colon (HCT116) 108121484
chr14 95981267 95981878 TCF7L2 GTRD no Colon (HCT116) 108121485
chr14 95981366 95981886 ZNF143 ENCODE Uniform TFBS no Embryonic Stem Cell Line (H1-hESC) 108121486
chr14 95981366 95981886 ZNF143 ENCODE Uniform TFBS no Embryonic Stem Cell Line (H1-hESC) 108121487
chr14 95981420 95981744 ZNF143 ENCODE Uniform TFBS no Embryonic Stem Cell Line (H1-hESC) 108121488
chr14 95981424 95981824 ZNF274 ENCODE Uniform TFBS no Liver (HepG2) 21636732
chr14 95981424 95981824 ZNF274 ENCODE Uniform TFBS no Liver (HepG2) 108121489
chr14 95981461 95981475 GLIS2 JASPAR yes 107604890
chr14 95981461 95981475 GLIS2 JASPAR yes 117497589
chr14 95981461 95981805 ZNF143 ENCODE Uniform TFBS no Embryonic Stem Cell Line (H1-hESC) 108121490

Genes associated with rs534946298[chr14:95981464], 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