| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:109302705-109303059 | Common:5; Rare:104 | ||||
| chr4:109433750-109433832 | Common:1; Rare:29 | ||||
| chr4:109703411-109703497 | Rare:32 | ||||
| chr4:109730057-109730202 | Common:2; Rare:28 | ||||
| chr4:109815380-109815815 | Common:2; Rare:110 | ||||
| chr4:110198486-110198667 | Rare:47 | ||||
| chr4:112231570-112232288 | Common:5; Rare:224 | ||||
| chr4:112636875-112637193 | Common:1; Rare:88 | ||||
| chr4:112637384-112637570 | Common:3; Rare:52 | ||||
| chr4:112817971-112818262 | Rare:45 | ||||
| chr4:113049207-113049437 | Rare:41 | ||||
| chr4:113049488-113049809 | Common:1; Rare:72; Clinvar:3; Clinvar (benign):2 | ||||
| chr4:113116808-113117092 | Common:1; Rare:41 | ||||
| chr4:113761129-113761232 | Rare:24 | ||||
| chr4:117085458-117085609 | Common:1; Rare:43 |