Enhancers that have rs112974464[chr19:557494]
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Chrom. Start End Enhancer ID Tissues that enhancer appears More
chr19 552765 561015 enh17834

Transcript factors that have rs112974464[chr19:557494]
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Chrom. Start End TF name Source Predicted site? Tissue id More
chr19 555359 557531 TCF7L2 GTRD no Colon (HCT116) 21829379
chr19 555359 557531 TCF7L2 GTRD no Colon (HCT116) 108344737
chr19 555425 557494 ZNF274 GTRD no Bone Marrow (K562) 21829386
chr19 555425 557494 ZNF274 GTRD no Bone Marrow (K562) 108344743
chr19 555561 557570 TCF7L2 GTRD no Colon (HCT116) 21829399
chr19 555561 557570 TCF7L2 GTRD no Colon (HCT116) 108344755
chr19 555785 557572 ZNF274 GTRD no Cervix (HeLa-S3) 21829451
chr19 555785 557572 ZNF274 GTRD no Cervix (HeLa-S3) 108344811
chr19 555799 557729 ZNF274 GTRD no Cervix (HeLa-S3) 21829452
chr19 555799 557729 ZNF274 GTRD no Cervix (HeLa-S3) 108344812
chr19 557157 557614 ZNF274 GTRD no Cervix (HeLa-S3) 21829655

Genes associated with rs112974464[chr19:557494], 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
chr19 1440838 1441937 + AC027307.3 ENSG00000268798.1 1440838 883344 Esophagus 0.237783 16748