Enhancers that have rs150269077[chr12:49708046]
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Chrom. Start End Enhancer ID Tissues that enhancer appears More
chr12 49706632 49711755 enh86104

Transcript factors that have rs150269077[chr12:49708046]
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Chrom. Start End TF name Source Predicted site? Tissue id More
chr12 49706391 49708069 TCF7L2 GTRD no Colon (HCT116) 21544679
chr12 49706467 49708235 TCF7L2 GTRD no Colon (HCT116) 21544681
chr12 49706501 49708152 TCF7L2 GTRD no Colon (HCT116) 21544684
chr12 49706814 49708221 TCF7L2 GTRD no Colon (HCT116) 21544687
chr12 49706972 49708139 TCF7L2 GTRD no Colon (HCT116) 21544688
chr12 49707078 49708105 TCF7L2 GTRD no Colon (HCT116) 21544690
chr12 49707098 49708337 ZNF274 GTRD no Cervix (HeLa-S3) 21544691
chr12 49707174 49708168 ZNF274 GTRD no Cervix (HeLa-S3) 21544693
chr12 49707295 49708346 ZNF274 GTRD no Cervix (HeLa-S3) 21544695
chr12 49707347 49708102 ZNF274 GTRD no Cervix (HeLa-S3) 21544700
chr12 49707508 49708160 ZNF274 GTRD no Cervix (HeLa-S3) 21544702
chr12 49707512 49708065 ZNF274 GTRD no Cervix (HeLa-S3) 21544704
chr12 49708037 49708048 FOXA1 JASPAR yes 120773272
chr12 49708038 49708049 FOXC1 JASPAR yes 120773273
chr12 49708038 49708050 FOXC2 JASPAR yes 120773274
chr12 49708043 49708056 ZBTB18 JASPAR yes 120773275

Genes associated with rs150269077[chr12:49708046], 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