Enhancers that have rs542389978[chr11:1040305]
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Chrom. Start End Enhancer ID Tissues that enhancer appears More

Transcript factors that have rs542389978[chr11:1040305]
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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 1039875 1040628 TCF7L2 GTRD no Colon (HCT116) 107950689
chr11 1039984 1042775 TCF7L2 GTRD no Colon (HCT116) 107950690
chr11 1040007 1040823 ZNF274 GTRD no Cervix (HeLa-S3) 107950691
chr11 1040068 1040445 ZNF274 GTRD no Cervix (HeLa-S3) 107950694
chr11 1040069 1040465 ZZZ3 ENCODE Uniform TFBS no Cervix (HeLa-S3) 107950695
chr11 1040091 1040607 ZZZ3 ENCODE Uniform TFBS no Cervix (HeLa-S3) 107950696
chr11 1040125 1040670 ZNF274 GTRD no Cervix (HeLa-S3) 107950697
chr11 1040132 1040662 ZZZ3 ENCODE Uniform TFBS no Cervix (HeLa-S3) 107950698
chr11 1040231 1040664 ERG GTRD no Prostate (RWPE1) 107950699

Genes associated with rs542389978[chr11:1040305], 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