Enhancers that have rs73400922[chr11:1547488]
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Chrom. Start End Enhancer ID Tissues that enhancer appears More

Transcript factors that have rs73400922[chr11:1547488]
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Chrom. Start End TF name Source Predicted site? Tissue id More
chr11 1545841 1549933 TCF7L2 GTRD no Colon (HCT116) 21465563
chr11 1545851 1550130 TCF7L2 GTRD no Colon (HCT116) 21465564
chr11 1545895 1549411 TCF7L2 GTRD no Colon (HCT116) 21465565
chr11 1545904 1550185 TCF7L2 GTRD no Colon (HCT116) 21465566
chr11 1545942 1549877 TCF7L2 GTRD no Colon (HCT116) 21465567
chr11 1546091 1548620 ZNF274 GTRD no Bone Marrow (K562) 21465568
chr11 1546254 1549197 TCF7L2 GTRD no Colon (HCT116) 21465571
chr11 1546268 1547784 ZNF274 GTRD no Bone Marrow (K562) 21465574
chr11 1546281 1550000 TCF7L2 GTRD no Colon (HCT116) 21465575
chr11 1546339 1547600 TCF7L2 GTRD no Colon (HCT116) 21465578
chr11 1546346 1547528 TCF7L2 GTRD no Colon (HCT116) 21465580
chr11 1546398 1549444 TCF7L2 GTRD no Colon (HCT116) 21465582
chr11 1546406 1547653 ZNF274 GTRD no Bone Marrow (K562) 21465583
chr11 1546465 1549131 TCF7L2 GTRD no Colon (HCT116) 21465591
chr11 1546498 1547547 TCF7L2 GTRD no Colon (HCT116) 21465594
chr11 1546591 1547504 TCF7L2 GTRD no Colon (HCT116) 21465609
chr11 1546593 1547646 TCF7L2 GTRD no Colon (HCT116) 21465610
chr11 1546953 1547604 TCF7L2 GTRD no Colon (HCT116) 21465628

Genes associated with rs73400922[chr11:1547488], 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
chr11 1411129 1483919 + BRSK2 ENSG00000174672.11 1411129 63569 Esophagus 0.00126261 10390