Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr9:109772222-109772424 | Rare:41 | ||||
chr9:113012157-113012308 | Rare:31 | ||||
chr9:113620609-113620837 | Common:2; Rare:46 | ||||
chr9:121599325-121599608 | Common:1; Rare:82 | ||||
chr9:123385460-123385680 | Rare:43 | ||||
chr9:124658269-124658443 | Rare:34 | ||||
chr9:124838161-124838323 | Common:4; Rare:39 | ||||
chr9:125473175-125473418 | Rare:41 | ||||
chr9:127741892-127742158 | Common:3; Rare:72 | ||||
chr9:127825544-127825751 | Common:2; Rare:62; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):3 | ||||
chr9:128838475-128838514 | Rare:11 | ||||
chr9:129174899-129175022 | Rare:26 | ||||
chr9:129208543-129208642 | Rare:21 | ||||
chr9:129320822-129321026 | Rare:34 | ||||
chr9:130712694-130712846 | Common:2; Rare:50 |