Enhancers that have rs569276700[chr16:89041695]
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Chrom. Start End Enhancer ID Tissues that enhancer appears More
chr16 89029754 89041849 enh47986

Transcript factors that have rs569276700[chr16:89041695]
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Chrom. Start End TF name Source Predicted site? Tissue id More
chr16 89035475 89042165 TCF7L2 GTRD no Colon (HCT116) 108224458
chr16 89035475 89042165 TCF7L2 GTRD no Colon (HCT116) 108224459
chr16 89035475 89042165 TCF7L2 GTRD no Colon (HCT116) 108224460
chr16 89037679 89042618 TCF7L2 GTRD no Colon (HCT116) 108224484
chr16 89037679 89042618 TCF7L2 GTRD no Colon (HCT116) 108224485
chr16 89037679 89042618 TCF7L2 GTRD no Colon (HCT116) 108224486
chr16 89040306 89041914 ZNF143 GTRD no Epithelial (MCF-7) 108224568
chr16 89040309 89041961 ZNF143 GTRD no Epithelial (MCF-7) 108224569
chr16 89040754 89043806 TCF7L2 GTRD no Colon (HCT116) 108224572
chr16 89041694 89041705 FOSL2 JASPAR yes 12312871
chr16 89041694 89041705 JUNB JASPAR yes 12312872
chr16 89041695 89041706 FOS JASPAR yes 12312873
chr16 89041695 89041706 FOSL1 JASPAR yes 12312874
chr16 89041695 89041706 JUND JASPAR yes 12312875
chr16 89041695 89041706 NFE2 JASPAR yes 12312876

Genes associated with rs569276700[chr16:89041695], 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