Enhancers that have rs148692315[chr12:107682796]
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Chrom. Start End Enhancer ID Tissues that enhancer appears More
chr12 107679505 107683755 enh80381
chr12 107682481 107682807 vista14784

Transcript factors that have rs148692315[chr12:107682796]
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Chrom. Start End TF name Source Predicted site? Tissue id More
chr12 107681490 107682921 ZNF274 GTRD no Liver (HepG2) 108056209
chr12 107681507 107683009 ZNF274 GTRD no Liver (HepG2) 108056211
chr12 107681517 107682823 ZNF274 GTRD no Liver (HepG2) 108056212
chr12 107681620 107682840 ZNF274 GTRD no Liver (HepG2) 108056213
chr12 107681650 107682882 ZNF274 GTRD no Liver (HepG2) 108056214
chr12 107681663 107683115 ZNF274 GTRD no Liver (HepG2) 108056216
chr12 107681765 107682915 ZNF274 GTRD no Liver (HepG2) 108056224
chr12 107681795 107682831 ZNF274 GTRD no Liver (HepG2) 108056227
chr12 107681876 107682911 ZNF274 GTRD no Liver (HepG2) 108056232
chr12 107682026 107682927 TCF7L2 GTRD no Colon (HCT116) 108056236
chr12 107682047 107682987 TCF7L2 GTRD no Colon (HCT116) 108056237
chr12 107682324 107683100 TCF7L2 GTRD no Colon (HCT116) 108056238
chr12 107682785 107682806 ZNF263 JASPAR yes 82471794
chr12 107682785 107682806 ZNF263 JASPAR yes 123544230
chr12 107682788 107682796 FEV JASPAR yes 82471796
chr12 107682788 107682796 FEV JASPAR yes 123544232
chr12 107682788 107682799 E2F4 JASPAR yes 82471797
chr12 107682788 107682799 E2F6 JASPAR yes 82471798
chr12 107682788 107682799 E2F4 JASPAR yes 123544233
chr12 107682788 107682799 E2F6 JASPAR yes 123544234
chr12 107682788 107682802 E2F7 JASPAR yes 82471799
chr12 107682788 107682802 E2F7 JASPAR yes 123544235
chr12 107682789 107682796 E2F1 TRANSFAC yes 82471800
chr12 107682789 107682796 E2F1 TRANSFAC yes 123544236
chr12 107682789 107682797 E2F1 JASPAR yes 82471801
chr12 107682789 107682797 E2F1 JASPAR yes 123544237
chr12 107682789 107682800 E2F1 JASPAR yes 82471802
chr12 107682789 107682800 E2F1 JASPAR yes 123544238
chr12 107682789 107682810 ZNF263 JASPAR yes 82471803
chr12 107682789 107682810 ZNF263 JASPAR yes 123544239

Genes associated with rs148692315[chr12:107682796], 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