| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:109815473-109815553 | Rare:25 | ||||
| chr4:110623067-110623277 | Common:1; Rare:44 | ||||
| chr4:112231593-112231831 | Common:2; Rare:74 | ||||
| chr4:112285789-112285986 | Rare:60 | ||||
| chr4:112636853-112637197 | Common:1; Rare:95 | ||||
| chr4:112637333-112637570 | Common:3; Rare:72 | ||||
| chr4:113761080-113761231 | Rare:43 | ||||
| chr4:113979009-113979181 | Common:3; Rare:28 | ||||
| chr4:113979602-113979816 | Common:6; Rare:49 | ||||
| chr4:117085511-117085581 | Common:1; Rare:18 | ||||
| chr4:118685286-118685471 | Common:3; Rare:58 | ||||
| chr4:118835945-118836219 | Common:1; Rare:63 | ||||
| chr4:119135756-119135923 | Common:1; Rare:24; Clinvar (benign):1 | ||||
| chr4:119212558-119212730 | Common:1; Rare:44 | ||||
| chr4:119213135-119213197 | Rare:10 |