| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:33025093-33025304 | Common:5; Rare:89 | ||||
| chr9:33290383-33290571 | Common:2; Rare:75 | ||||
| chr9:33402505-33402795 | Rare:56 | ||||
| chr9:33473881-33474078 | Common:2; Rare:61 | ||||
| chr9:34049181-34049263 | Common:1; Rare:20 | ||||
| chr9:34329198-34329620 | Common:1; Rare:131 | ||||
| chr9:34590331-34590558 | Common:4; Rare:48 | ||||
| chr9:35161832-35162038 | Common:4; Rare:57 | ||||
| chr9:35657857-35658376 | Common:8; Rare:433; Clinvar:41; Clinvar (benign):15; Clinvar (pathogenic):40 | ||||
| chr9:35685432-35685789 | Common:1; Rare:84; Clinvar:1; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr9:35689702-35690037 | Common:3; Rare:109; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr9:35690109-35690342 | Common:1; Rare:65 | ||||
| chr9:35732082-35732339 | Common:2; Rare:72 | ||||
| chr9:35732373-35732676 | Common:2; Rare:76 | ||||
| chr9:35748965-35749362 | Common:2; Rare:147 |