Enhancers that have rs12462766[chr19:417737]
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Chrom. Start End Enhancer ID Tissues that enhancer appears More

Transcript factors that have rs12462766[chr19:417737]
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Chrom. Start End TF name Source Predicted site? Tissue id More
chr19 416678 418430 TCF7L2 GTRD no Colon (HCT116) 108343741
chr19 416885 418650 TCF7L2 GTRD no Colon (HCT116) 108343742
chr19 417023 419574 TCF7L2 GTRD no Colon (HCT116) 108343743
chr19 417075 417873 TCF7L2 GTRD no Colon (HCT116) 108343744
chr19 417564 418125 ZNF143 GTRD no Epithelial (MCF-7) 108343745
chr19 417570 418162 ZNF143 GTRD no Epithelial (MCF-7) 108343746
chr19 417668 418099 TCF7L2 GTRD no Colon (HCT116) 108343747
chr19 417730 418054 ZNF143 ENCODE Uniform TFBS no Embryonic Stem Cell Line (H1-hESC) 108343748

Genes associated with rs12462766[chr19:417737], 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