| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:109703391-109703641 | Common:1; Rare:84 | ||||
| chr4:109729923-109730218 | Common:4; Rare:74 | ||||
| chr4:109815464-109815798 | Common:1; Rare:89 | ||||
| chr4:110198494-110198627 | Rare:37 | ||||
| chr4:112231586-112231882 | Common:2; Rare:93 | ||||
| chr4:112232129-112232276 | Common:1; Rare:62 | ||||
| chr4:112636850-112637204 | Common:2; Rare:98 | ||||
| chr4:112637380-112637576 | Common:3; Rare:55 | ||||
| chr4:112817977-112818118 | Rare:21 | ||||
| chr4:113145661-113145792 | Rare:27 | ||||
| chr4:113761075-113761226 | Rare:44 | ||||
| chr4:117085494-117085602 | Common:1; Rare:30 | ||||
| chr4:118685271-118685440 | Common:3; Rare:58 | ||||
| chr4:118835952-118836219 | Common:1; Rare:61 | ||||
| chr4:119135756-119135923 | Common:1; Rare:24; Clinvar (benign):1 |