| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:19378457-19378930 | Common:1; Rare:143 | ||||
| chr9:25677517-25677673 | Common:1; Rare:74 | ||||
| chr9:32431470-32431751 | Common:1; Rare:63 | ||||
| chr9:32550831-32551077 | Common:1; Rare:106; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:35604027-35604212 | Common:3; Rare:48 | ||||
| chr9:35740985-35741187 | Rare:51; Clinvar (benign):3 | ||||
| chr9:37776223-37776350 | Common:1; Rare:44 | ||||
| chr9:39809317-39809513 | Common:4; Rare:16 | ||||
| chr9:39809851-39809865 | Common:1 | ||||
| chr9:39810022-39810056 | Rare:1 | ||||
| chr9:40584157-40584477 | Rare:4 | ||||
| chr9:40991963-40992479 | Common:7; Rare:36 | ||||
| chr9:41358575-41358916 | Common:2; Rare:82 | ||||
| chr9:62897686-62897712 | Common:1; Rare:6 | ||||
| chr9:63334357-63334718 | Common:1; Rare:20 |