| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:95548992-95549123 | Rare:31 | ||||
| chr4:95549189-95549284 | Common:1; Rare:13 | ||||
| chr4:98143450-98143588 | Rare:34 | ||||
| chr4:98261142-98261519 | Common:1; Rare:127 | ||||
| chr4:98658601-98658919 | Common:2; Rare:90 | ||||
| chr4:98929096-98929382 | Common:3; Rare:72 | ||||
| chr4:99088696-99088891 | Common:6; Rare:90 | ||||
| chr4:99352707-99353015 | Common:1; Rare:70 | ||||
| chr4:99563593-99563772 | Common:2; Rare:49 | ||||
| chr4:99563989-99564143 | Common:2; Rare:50; Clinvar:2; Clinvar (benign):2 | ||||
| chr4:99894333-99894625 | Common:3; Rare:98 | ||||
| chr4:99949735-99949991 | Common:3; Rare:90 | ||||
| chr4:99950239-99950485 | Rare:52 | ||||
| chr4:101347543-101347822 | Common:4; Rare:83 | ||||
| chr4:102431227-102431298 | Common:1; Rare:12 |