Enhancers that have rs199827975[chr19:460292]
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Chrom. Start End Enhancer ID Tissues that enhancer appears More

Transcript factors that have rs199827975[chr19:460292]
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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

Genes associated with rs199827975[chr19:460292], 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
chr19 416583 460996 - SHC2 ENSG00000129946.6 460996 0 Esophagus 1.67849e-18 16701
chr19 416583 460996 - SHC2 ENSG00000129946.6 460996 0 Spleen 2.29553e-06 16701