| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:95051620-95051691 | Rare:16 | ||||
| chr4:95548763-95549149 | Common:2; Rare:121 | ||||
| chr4:95549196-95549300 | Common:1; Rare:18 | ||||
| chr4:98143432-98143649 | Common:1; Rare:56 | ||||
| chr4:98261142-98261568 | Common:1; Rare:147 | ||||
| chr4:98657641-98657830 | Rare:39 | ||||
| chr4:98658609-98658760 | Common:1; Rare:44 | ||||
| chr4:98929001-98929242 | Common:3; Rare:81 | ||||
| chr4:98995491-98995797 | Common:6; Rare:107 | ||||
| chr4:99088696-99088891 | Common:6; Rare:90 | ||||
| chr4:99563557-99563794 | Common:2; Rare:64 | ||||
| chr4:99563924-99564173 | Common:2; Rare:82; Clinvar:2; Clinvar (benign):2 | ||||
| chr4:99894347-99894628 | Common:3; Rare:95 | ||||
| chr4:99949694-99949964 | Common:3; Rare:95 | ||||
| chr4:99950242-99950488 | Rare:51 |