| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:22009296-22009472 | Common:1; Rare:53 | ||||
| chr9:26947132-26947232 | Rare:35 | ||||
| chr9:26956246-26956440 | Common:2; Rare:73 | ||||
| chr9:32384479-32384724 | Common:1; Rare:90 | ||||
| chr9:33025093-33025290 | Common:5; Rare:79 | ||||
| chr9:33076626-33076850 | Common:2; Rare:75 | ||||
| chr9:33750552-33750720 | Rare:50 | ||||
| chr9:34048866-34048992 | Common:1; Rare:51 | ||||
| chr9:34329186-34329588 | Rare:126 | ||||
| chr9:34646544-34646684 | Common:1; Rare:36; Clinvar:2 | ||||
| chr9:35103100-35103198 | Common:1; Rare:30 | ||||
| chr9:35657881-35658352 | Common:7; Rare:399; Clinvar:35; Clinvar (benign):14; Clinvar (pathogenic):37 | ||||
| chr9:35673874-35673933 | Common:2; Rare:18 | ||||
| chr9:35732096-35732320 | Rare:65 | ||||
| chr9:35732523-35732668 | Common:1; Rare:39 |