| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:6757865-6758060 | Common:4; Rare:75 | ||||
| chr9:13279616-13279811 | Common:2; Rare:61 | ||||
| chr9:15307330-15307444 | Rare:50 | ||||
| chr9:16870657-16870838 | Rare:88 | ||||
| chr9:17134884-17135063 | Rare:83 | ||||
| chr9:18473944-18474178 | Rare:59 | ||||
| chr9:26947151-26947339 | Rare:60 | ||||
| chr9:33001560-33001846 | Common:3; Rare:123; Clinvar (benign):3 | ||||
| chr9:33025092-33025304 | Common:6; Rare:89 | ||||
| chr9:33166867-33166956 | Rare:35 | ||||
| chr9:33290255-33290565 | Common:3; Rare:104 | ||||
| chr9:33473892-33474143 | Common:2; Rare:66 | ||||
| chr9:34048880-34048973 | Rare:37 | ||||
| chr9:34329257-34329593 | Rare:99 | ||||
| chr9:34458563-34458833 | Common:1; Rare:63; Clinvar:1; Clinvar (benign):1 |