| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:33025677-33025853 | Common:3; Rare:79 | ||||
| chr9:33076610-33076877 | Common:2; Rare:93 | ||||
| chr9:33166881-33166956 | Rare:32 | ||||
| chr9:33290394-33290575 | Common:2; Rare:69 | ||||
| chr9:33750532-33750690 | Rare:49 | ||||
| chr9:34048839-34048953 | Common:1; Rare:53 | ||||
| chr9:34049175-34049263 | Common:1; Rare:22 | ||||
| chr9:34178933-34179072 | Common:1; Rare:38 | ||||
| chr9:34329186-34329598 | Rare:131 | ||||
| chr9:34458539-34458968 | Common:1; Rare:100; Clinvar:5; Clinvar (benign):1 | ||||
| chr9:34612079-34612197 | Common:5; Rare:40 | ||||
| chr9:34646544-34646798 | Common:1; Rare:78; Clinvar:4; Clinvar (pathogenic):3 | ||||
| chr9:34652018-34652207 | Rare:53 | ||||
| chr9:34665373-34665660 | Rare:94 | ||||
| chr9:34989435-34989781 | Common:2; Rare:91 |