Enhancers that have rs543692248[chr19:461503]
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Chrom. Start End Enhancer ID Tissues that enhancer appears More

Transcript factors that have rs543692248[chr19:461503]
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Chrom. Start End TF name Source Predicted site? Tissue id More
chr19 459410 462486 ZNF274 GTRD no Bone Marrow (K562) 108343761
chr19 459431 462639 TCF7L2 GTRD no Colon (HCT116) 108343762
chr19 459554 462770 ZNF274 GTRD no Bone Marrow (K562) 108343763
chr19 459590 462570 TCF7L2 GTRD no Colon (HCT116) 108343764
chr19 459642 462682 TCF7L2 GTRD no Colon (HCT116) 108343765
chr19 459642 462807 TCF7L2 GTRD no Colon (HCT116) 108343766
chr19 459656 462658 TCF7L2 GTRD no Colon (HCT116) 108343767
chr19 459683 462703 ZNF274 GTRD no Liver (HepG2) 108343768
chr19 459838 462603 TCF7L2 GTRD no Colon (HCT116) 108343769
chr19 460026 462291 TCF7L2 GTRD no Colon (HCT116) 108343770
chr19 460825 462425 TCF7L2 GTRD no Colon (HCT116) 108343771
chr19 460842 462365 ZNF274 GTRD no Liver (HepG2) 108343772
chr19 461294 462390 ZNF274 GTRD no Liver (HepG2) 108343773
chr19 461311 462576 ZNF274 GTRD no Bone Marrow (K562) 108343774
chr19 461324 462441 ZNF274 GTRD no Liver (HepG2) 108343775
chr19 461497 462167 ZNF143 ENCODE Uniform TFBS no Embryonic Stem Cell Line (H1-hESC) 108343776

Genes associated with rs543692248[chr19:461503], 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