Enhancers that have rs78591747[chr17:27359832]
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Chrom. Start End Enhancer ID Tissues that enhancer appears More
chr17 27357045 27369515 enh69254
chr17 27359808 27360065 vista24320

Transcript factors that have rs78591747[chr17:27359832]
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Chrom. Start End TF name Source Predicted site? Tissue id More
chr17 27359229 27359899 ZNF143 ENCODE Uniform TFBS no Embryonic Stem Cell Line (H1-hESC) 108246384
chr17 27359378 27359988 ZNF143 ENCODE Uniform TFBS no Embryonic Stem Cell Line (H1-hESC) 108246385
chr17 27359716 27360233 TCF7L2 GTRD no Colon (HCT116) 108246386
chr17 27359764 27360088 ZNF143 ENCODE Uniform TFBS no Embryonic Stem Cell Line (H1-hESC) 108246387
chr17 27359802 27360112 ZNF143 ENCODE Uniform TFBS no Embryonic Stem Cell Line (H1-hESC) 108246388
chr17 27359804 27360060 ZNF143 ENCODE Uniform TFBS no Embryonic Stem Cell Line (H1-hESC) 108246389
chr17 27359816 27360076 ZNF143 ENCODE Uniform TFBS no Embryonic Stem Cell Line (H1-hESC) 108246390

Genes associated with rs78591747[chr17:27359832], 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
chr17 26934982 26941218 - SGK494 ENSG00000167524.10 26941218 418614 Esophagus 0.138241 15578