Enhancers that have rs376669882[chr12:46468796]
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Chrom. Start End Enhancer ID Tissues that enhancer appears More

Transcript factors that have rs376669882[chr12:46468796]
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Chrom. Start End TF name Source Predicted site? Tissue id More
chr12 46467679 46468813 TCF7L2 GTRD no Colon (HCT116) 21540544
chr12 46467826 46469086 TCF7L2 GTRD no Colon (HCT116) 21540545
chr12 46467900 46468939 TCF7L2 GTRD no Colon (HCT116) 21540546
chr12 46467999 46469019 ZNF274 GTRD no Cervix (HeLa-S3) 21540548
chr12 46467999 46469029 ZNF274 GTRD no Cervix (HeLa-S3) 21540549
chr12 46468096 46468925 ZNF274 GTRD no Cervix (HeLa-S3) 21540552
chr12 46468098 46468903 ZNF274 GTRD no Cervix (HeLa-S3) 21540553
chr12 46468104 46468919 ZNF274 GTRD no Cervix (HeLa-S3) 21540555
chr12 46468132 46468828 ZNF274 GTRD no Cervix (HeLa-S3) 21540558
chr12 46468158 46469087 ZNF274 GTRD no Cervix (HeLa-S3) 21540561

Genes associated with rs376669882[chr12:46468796], 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