Enhancers that have rs116886445[chr19:3403753]
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Chrom. Start End Enhancer ID Tissues that enhancer appears More
chr19 3395005 3410358 enh17863

Transcript factors that have rs116886445[chr19:3403753]
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Chrom. Start End TF name Source Predicted site? Tissue id More
chr19 3402647 3405571 TCF7L2 GTRD no Colon (HCT116) 21839354
chr19 3402647 3405571 TCF7L2 GTRD no Colon (HCT116) 108366699
chr19 3402647 3405571 TCF7L2 GTRD no Colon (HCT116) 108366700
chr19 3402647 3405571 TCF7L2 GTRD no Colon (HCT116) 108366701
chr19 3403375 3405612 TCF7L2 GTRD no Colon (HCT116) 21839355
chr19 3403375 3405612 TCF7L2 GTRD no Colon (HCT116) 108366702
chr19 3403375 3405612 TCF7L2 GTRD no Colon (HCT116) 108366703
chr19 3403375 3405612 TCF7L2 GTRD no Colon (HCT116) 108366704
chr19 3403464 3405554 TCF7L2 GTRD no Colon (HCT116) 21839356
chr19 3403464 3405554 TCF7L2 GTRD no Colon (HCT116) 108366705
chr19 3403464 3405554 TCF7L2 GTRD no Colon (HCT116) 108366706
chr19 3403464 3405554 TCF7L2 GTRD no Colon (HCT116) 108366707
chr19 3403502 3405348 TCF7L2 GTRD no Colon (HCT116) 21839357
chr19 3403502 3405348 TCF7L2 GTRD no Colon (HCT116) 108366708
chr19 3403502 3405348 TCF7L2 GTRD no Colon (HCT116) 108366709
chr19 3403502 3405348 TCF7L2 GTRD no Colon (HCT116) 108366710
chr19 3403570 3405416 TCF7L2 GTRD no Colon (HCT116) 21839358
chr19 3403570 3405416 TCF7L2 GTRD no Colon (HCT116) 108366711
chr19 3403570 3405416 TCF7L2 GTRD no Colon (HCT116) 108366712
chr19 3403570 3405416 TCF7L2 GTRD no Colon (HCT116) 108366713
chr19 3403648 3405195 TCF7L2 GTRD no Colon (HCT116) 21839359
chr19 3403648 3405195 TCF7L2 GTRD no Colon (HCT116) 108366714
chr19 3403648 3405195 TCF7L2 GTRD no Colon (HCT116) 108366715
chr19 3403648 3405195 TCF7L2 GTRD no Colon (HCT116) 108366716
chr19 3403724 3404940 TCF7L2 GTRD no Colon (HCT116) 21839360
chr19 3403724 3404940 TCF7L2 GTRD no Colon (HCT116) 108366717
chr19 3403724 3404940 TCF7L2 GTRD no Colon (HCT116) 108366718
chr19 3403738 3403753 ZIC4 JASPAR yes 112128652
chr19 3403753 3403758 MYC TRANSFAC yes 112128654

Genes associated with rs116886445[chr19:3403753], 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