| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:143515922-143516097 | Rare:35 | ||||
| chr8:145002844-145003056 | Common:2; Rare:70 | ||||
| chr9:569449-569541 | Common:1; Rare:34 | ||||
| chr9:5627233-5627383 | Rare:33 | ||||
| chr9:5629711-5629947 | Rare:61 | ||||
| chr9:6681620-6681741 | Common:1; Rare:49 | ||||
| chr9:6704187-6704343 | Common:3; Rare:61 | ||||
| chr9:22512606-22512698 | Rare:19 | ||||
| chr9:22517200-22517330 | Rare:36 | ||||
| chr9:32550839-32551187 | Common:1; Rare:140; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:33446407-33446628 | Common:2; Rare:40 | ||||
| chr9:36765855-36765917 | Rare:11 | ||||
| chr9:37004587-37004781 | Common:1; Rare:34 | ||||
| chr9:37032890-37033007 | Common:2; Rare:28 | ||||
| chr9:37036456-37036618 | Rare:35 |