| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:88284534-88284768 | Common:1; Rare:53 | ||||
| chr4:88592323-88592542 | Rare:71 | ||||
| chr4:88697751-88697909 | Common:2; Rare:58 | ||||
| chr4:88759447-88759728 | Rare:48 | ||||
| chr4:89111358-89111577 | Common:4; Rare:83 | ||||
| chr4:89836856-89837253 | Common:3; Rare:125; Clinvar:5; Clinvar (benign):1 | ||||
| chr4:94207528-94207649 | Rare:38 | ||||
| chr4:95548912-95549140 | Common:2; Rare:49 | ||||
| chr4:95549196-95549334 | Common:1; Rare:24 | ||||
| chr4:98143464-98143640 | Common:1; Rare:43 | ||||
| chr4:98261171-98261499 | Common:1; Rare:100 | ||||
| chr4:98929108-98929378 | Common:3; Rare:68 | ||||
| chr4:98995463-98995756 | Common:6; Rare:108 | ||||
| chr4:99088704-99088891 | Common:6; Rare:82 | ||||
| chr4:99563989-99564127 | Common:2; Rare:45; Clinvar:1; Clinvar (benign):2 |