| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:27573429-27573551 | Common:5; Rare:75 | ||||
| chr9:32384417-32384732 | Common:1; Rare:110 | ||||
| chr9:32526171-32526344 | Common:4; Rare:50 | ||||
| chr9:32573073-32573199 | Common:2; Rare:48 | ||||
| chr9:33025071-33025383 | Common:7; Rare:127 | ||||
| chr9:33076610-33076877 | Common:2; Rare:93 | ||||
| chr9:33166889-33166956 | Rare:28 | ||||
| chr9:33290255-33290570 | Common:3; Rare:107 | ||||
| chr9:33817611-33817890 | Common:2; Rare:80 | ||||
| chr9:34048870-34048992 | Common:1; Rare:49 | ||||
| chr9:34049186-34049267 | Common:1; Rare:19 | ||||
| chr9:34329179-34329638 | Common:1; Rare:143 | ||||
| chr9:34458533-34458840 | Common:2; Rare:75; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:34652015-34652208 | Rare:55 | ||||
| chr9:35103078-35103297 | Common:1; Rare:78 |