Enhancers that have rs34118992[chr12:49706746]
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Chrom. Start End Enhancer ID Tissues that enhancer appears More
chr12 49706632 49711755 enh86104

Transcript factors that have rs34118992[chr12:49706746]
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Chrom. Start End TF name Source Predicted site? Tissue id More
chr12 49705971 49706864 ZNF274 GTRD no Cervix (HeLa-S3) 21544676
chr12 49706340 49708014 TCF7L2 GTRD no Colon (HCT116) 21544677
chr12 49706389 49708036 TCF7L2 GTRD no Colon (HCT116) 21544678
chr12 49706391 49708069 TCF7L2 GTRD no Colon (HCT116) 21544679
chr12 49706456 49707905 TCF7L2 GTRD no Colon (HCT116) 21544680
chr12 49706467 49708235 TCF7L2 GTRD no Colon (HCT116) 21544681
chr12 49706472 49707881 TCF7L2 GTRD no Colon (HCT116) 21544682
chr12 49706476 49707933 TCF7L2 GTRD no Colon (HCT116) 21544683
chr12 49706501 49708152 TCF7L2 GTRD no Colon (HCT116) 21544684
chr12 49706589 49707936 ZNF274 GTRD no Cervix (HeLa-S3) 21544685
chr12 49706719 49707825 TCF7L2 GTRD no Colon (HCT116) 21544686
chr12 49706738 49706749 TBX2 JASPAR yes 120772954
chr12 49706738 49706751 EOMES JASPAR yes 120772955
chr12 49706741 49706756 MEF2C JASPAR yes 120772956
chr12 49706744 49706759 FOXP1 JASPAR yes 120772957
chr12 49706746 49706761 FOXP1 JASPAR yes 120772958

Genes associated with rs34118992[chr12:49706746], 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