| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:43124572-43124666 | Rare:18 | ||||
| chr8:43124701-43124995 | Common:1; Rare:62 | ||||
| chr8:43129120-43129437 | Rare:59 | ||||
| chr8:43129823-43129938 | Rare:21 | ||||
| chr8:43130172-43130274 | Rare:12 | ||||
| chr8:43130731-43131137 | Common:2; Rare:74 | ||||
| chr8:43197687-43197935 | Common:2; Rare:69; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr8:47353193-47353507 | Rare:56 | ||||
| chr8:47353728-47354045 | Rare:54 | ||||
| chr8:47383346-47383431 | Common:1; Rare:16 | ||||
| chr8:47385597-47385626 | Rare:12 | ||||
| chr8:47454664-47454777 | Rare:18 | ||||
| chr8:47592636-47592829 | Rare:46 | ||||
| chr8:47736756-47737226 | Common:4; Rare:123 | ||||
| chr8:47737257-47737307 | Rare:18 |