Enhancers that have rs12149025[chr16:89049973]
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Chrom. Start End Enhancer ID Tissues that enhancer appears More
chr16 89046288 89055611 enh47987
chr16 89049819 89050070 vista23539

Transcript factors that have rs12149025[chr16:89049973]
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Chrom. Start End TF name Source Predicted site? Tissue id More
chr16 89047034 89056300 TCF7L2 GTRD no Colon (HCT116) 108224658
chr16 89047034 89056300 TCF7L2 GTRD no Colon (HCT116) 108224659
chr16 89047034 89056300 TCF7L2 GTRD no Colon (HCT116) 108224660
chr16 89047034 89056300 TCF7L2 GTRD no Colon (HCT116) 108224661
chr16 89047034 89056300 TCF7L2 GTRD no Colon (HCT116) 108224662
chr16 89047135 89056347 TCF7L2 GTRD no Colon (HCT116) 108224663
chr16 89047135 89056347 TCF7L2 GTRD no Colon (HCT116) 108224664
chr16 89047135 89056347 TCF7L2 GTRD no Colon (HCT116) 108224665
chr16 89047135 89056347 TCF7L2 GTRD no Colon (HCT116) 108224666
chr16 89047135 89056347 TCF7L2 GTRD no Colon (HCT116) 108224667
chr16 89047179 89056338 TCF7L2 GTRD no Colon (HCT116) 108224670
chr16 89047179 89056338 TCF7L2 GTRD no Colon (HCT116) 108224671
chr16 89047179 89056338 TCF7L2 GTRD no Colon (HCT116) 108224672
chr16 89047179 89056338 TCF7L2 GTRD no Colon (HCT116) 108224673
chr16 89047179 89056338 TCF7L2 GTRD no Colon (HCT116) 108224674
chr16 89049349 89050575 TCF7L2 GTRD no Colon (HCT116) 108224731
chr16 89049349 89050575 TCF7L2 GTRD no Colon (HCT116) 108224732
chr16 89049349 89050575 TCF7L2 GTRD no Colon (HCT116) 108224733
chr16 89049473 89050297 TCF7L2 GTRD no Colon (HCT116) 108224735
chr16 89049473 89050297 TCF7L2 GTRD no Colon (HCT116) 108224736
chr16 89049670 89050309 ZNF274 GTRD no Blood (GM12878) 108224737
chr16 89049670 89050309 ZNF274 GTRD no Blood (GM12878) 108224738
chr16 89049815 89050097 ZNF274 GTRD no Liver (HepG2) 108224739
chr16 89049881 89050121 ZZZ3 ENCODE Uniform TFBS no Blood (GM12878) 108224740
chr16 89049905 89055158 TCF7L2 GTRD no Colon (HCT116) 108224741
chr16 89049905 89055158 TCF7L2 GTRD no Colon (HCT116) 108224742
chr16 89049905 89055158 TCF7L2 GTRD no Colon (HCT116) 108224743

Genes associated with rs12149025[chr16:89049973], 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