Enhancers that have rs181304488[chr11:1039967]
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Chrom. Start End Enhancer ID Tissues that enhancer appears More
chr11 1039894 1040259 vista9324

Transcript factors that have rs181304488[chr11:1039967]
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Chrom. Start End TF name Source Predicted site? Tissue id More
chr11 1038610 1043164 TCF7L2 GTRD no Colon (HCT116) 107950680
chr11 1039234 1040408 TCF7L2 GTRD no Colon (HCT116) 107950681
chr11 1039258 1041157 ZNF274 GTRD no Cervix (HeLa-S3) 107950682
chr11 1039259 1040719 TCF7L2 GTRD no Colon (HCT116) 107950683
chr11 1039631 1040323 TCF7L2 GTRD no Colon (HCT116) 107950685
chr11 1039654 1042622 ZNF274 GTRD no Cervix (HeLa-S3) 107950686
chr11 1039686 1041194 ZNF274 GTRD no Cervix (HeLa-S3) 107950687
chr11 1039722 1040155 TCF7L2 GTRD no Colon (HCT116) 107950688
chr11 1039875 1040628 TCF7L2 GTRD no Colon (HCT116) 107950689
chr11 1039959 1039969 SP1 JASPAR yes 114026722
chr11 1039960 1039981 REST JASPAR yes 114026723
chr11 1039961 1039980 REST JASPAR yes 114026724
chr11 1039962 1039968 NFE2 TRANSFAC yes 114026725

Genes associated with rs181304488[chr11:1039967], 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