Enhancers that have rs182690835[chr12:66174908]
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Chrom. Start End Enhancer ID Tissues that enhancer appears More
chr12 66168947 66177881 enh58441

Transcript factors that have rs182690835[chr12:66174908]
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Chrom. Start End TF name Source Predicted site? Tissue id More
chr12 66174168 66175383 TCF7L2 GTRD no Colon (HCT116) 21553383
chr12 66174309 66175321 TCF7L2 GTRD no Colon (HCT116) 21553384
chr12 66174334 66175446 TCF7L2 GTRD no Colon (HCT116) 21553385
chr12 66174388 66175258 TCF7L2 GTRD no Colon (HCT116) 21553386
chr12 66174643 66175237 TCF7L2 GTRD no Colon (HCT116) 21553387
chr12 66174700 66175234 TCF7L2 GTRD no Colon (HCT116) 21553388
chr12 66174902 66174916 ONECUT1 JASPAR yes 121493146
chr12 66174903 66174913 CUX1 JASPAR yes 121493147
chr12 66174903 66174913 CUX2 JASPAR yes 121493148
chr12 66174903 66174913 PAX7 JASPAR yes 121493149
chr12 66174908 66174923 STAT1 JASPAR yes 121493150

Genes associated with rs182690835[chr12:66174908], 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