Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:86956225-86956263 | Rare:6 | ||||
chr11:101128214-101128357 | Rare:52 | ||||
chr11:112028549-112028870 | Rare:72; Clinvar:1; Clinvar (benign):6 | ||||
chr11:114160074-114160357 | Common:1; Rare:60 | ||||
chr11:114161164-114161394 | Common:3; Rare:37 | ||||
chr11:118791699-118791845 | Rare:46 | ||||
chr11:119312055-119312359 | Common:1; Rare:105 | ||||
chr11:119314689-119314908 | Rare:69 | ||||
chr11:123358526-123358566 | Rare:7 | ||||
chr11:130522334-130522581 | Common:1; Rare:51 | ||||
chr12:581212-581507 | Common:4; Rare:46 | ||||
chr12:716562-716763 | Common:1; Rare:23 | ||||
chr12:3071126-3071203 | Rare:18 | ||||
chr12:6582650-6582933 | Rare:64 | ||||
chr12:7089354-7089726 | Common:3; Rare:124 |