Enhancers that have rs569305748[chr17:39953787]
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Chrom. Start End Enhancer ID Tissues that enhancer appears More
chr17 39947125 39957819 enh17155

Transcript factors that have rs569305748[chr17:39953787]
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Chrom. Start End TF name Source Predicted site? Tissue id More
chr17 39951896 39953988 TCF7L2 GTRD no Colon (HCT116) 21758369
chr17 39952025 39953870 TCF7L2 GTRD no Colon (HCT116) 21758370
chr17 39952037 39953948 TCF7L2 GTRD no Colon (HCT116) 21758371
chr17 39952102 39953795 TCF7L2 GTRD no Colon (HCT116) 21758373
chr17 39952239 39954156 TCF7L2 GTRD no Colon (HCT116) 21758374
chr17 39952255 39953814 TCF7L2 GTRD no Colon (HCT116) 21758376
chr17 39952346 39954000 TCF7L2 GTRD no Colon (HCT116) 21758378
chr17 39952494 39953846 TCF7L2 GTRD no Colon (HCT116) 21758382
chr17 39952531 39953788 ZNF143 GTRD no Epithelial (MCF-7) 21758384
chr17 39952555 39953808 TCF7L2 GTRD no Colon (HCT116) 21758386
chr17 39953284 39954213 TCF7L2 GTRD no Colon (HCT116) 21758394
chr17 39953774 39953794 ESR1 JASPAR yes 54277138
chr17 39953774 39953795 ZNF263 JASPAR yes 54277139
chr17 39953782 39953796 PLAG1 JASPAR yes 54277140
chr17 39953782 39953803 ZNF263 JASPAR yes 54277141
chr17 39953785 39953795 SP1 JASPAR yes 54277142

Genes associated with rs569305748[chr17:39953787], 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