| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:113929501-113929878 | Common:4; Rare:99 | ||||
| chr1:113979252-113979564 | Common:1; Rare:75 | ||||
| chr1:114780511-114780805 | Common:1; Rare:110 | ||||
| chr1:115089428-115089633 | Common:3; Rare:79 | ||||
| chr1:115976328-115976567 | Rare:80 | ||||
| chr1:115976797-115976902 | Rare:29 | ||||
| chr1:116373038-116373439 | Common:1; Rare:134 | ||||
| chr1:116398764-116399084 | Common:1; Rare:69 | ||||
| chr1:116399207-116399542 | Rare:57 | ||||
| chr1:116570916-116571190 | Common:3; Rare:81 | ||||
| chr1:116754351-116754495 | Rare:40 | ||||
| chr1:117060072-117060349 | Common:6; Rare:64 | ||||
| chr1:117367297-117367610 | Common:5; Rare:108 | ||||
| chr1:117929532-117929807 | Common:4; Rare:82 | ||||
| chr1:119140574-119140790 | Common:1; Rare:82; Clinvar (pathogenic):1 |