EnhancerDB
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  3. rs569245332[chr12:48994734]
Enhancers that have rs569245332[chr12:48994734]
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Chrom. Start End Enhancer ID Tissues that enhancer appears More
chr12 48992434 48998192 enh68136
Bone Marrow (K562) Colon (HCT116) Neural Stem Cells (H9)
Transcript factors that have rs569245332[chr12:48994734]
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Chrom. Start End TF name Source Predicted site? Tissue id More
chr12 48993790 48994822 TCF7L2 GTRD no Colon (HCT116) 21544170
chr12 48994378 48995164 TCF7L2 GTRD no Colon (HCT116) 21544171
chr12 48994434 48996054 TCF7L2 GTRD no Colon (HCT116) 21544172
chr12 48994485 48995111 TCF7L2 GTRD no Colon (HCT116) 21544173
chr12 48994534 48995256 TCF7L2 GTRD no Colon (HCT116) 21544174
chr12 48994544 48995063 TCF7L2 GTRD no Colon (HCT116) 21544175
chr12 48994546 48995128 TCF7L2 GTRD no Colon (HCT116) 21544176
chr12 48994563 48995166 TCF7L2 GTRD no Colon (HCT116) 21544177
chr12 48994722 48994734 POU2F1 JASPAR yes 120747290
chr12 48994722 48994735 POU3F3 JASPAR yes 120747291
chr12 48994722 48994736 POU1F1 JASPAR yes 120747292
chr12 48994723 48994735 POU3F1 JASPAR yes 120747293
chr12 48994723 48994735 POU3F2 JASPAR yes 120747294
chr12 48994723 48994736 POU2F2 JASPAR yes 120747295
Genes associated with rs569245332[chr12:48994734], 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