| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:35341751-35341909 | Common:1; Rare:25 | ||||
| chr9:35491658-35491906 | Common:1; Rare:40 | ||||
| chr9:35491914-35491977 | Common:1; Rare:7 | ||||
| chr9:35604027-35604220 | Common:3; Rare:51 | ||||
| chr9:35604261-35604453 | Rare:38 | ||||
| chr9:35724571-35724956 | Common:1; Rare:85 | ||||
| chr9:35909372-35909508 | Common:2; Rare:30 | ||||
| chr9:36236915-36237038 | Rare:29; Clinvar (benign):1; Clinvar (pathogenic):3 | ||||
| chr9:39809654-39809781 | Common:2; Rare:11 | ||||
| chr9:40106586-40106897 | Common:3; Rare:28 | ||||
| chr9:40991976-40992428 | Common:7; Rare:30 | ||||
| chr9:41073629-41073731 | Common:1; Rare:14 | ||||
| chr9:41074514-41074689 | Common:1; Rare:36 | ||||
| chr9:41074946-41075201 | Common:3; Rare:38 | ||||
| chr9:41358755-41358942 | Common:2; Rare:53 |