| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:35103049-35103297 | Common:1; Rare:94 | ||||
| chr9:35657863-35658342 | Common:7; Rare:410; Clinvar:39; Clinvar (benign):14; Clinvar (pathogenic):40 | ||||
| chr9:35665171-35665276 | Rare:44 | ||||
| chr9:35689792-35690123 | Common:4; Rare:109; Clinvar:4; Clinvar (benign):1 | ||||
| chr9:35732076-35732334 | Common:2; Rare:70 | ||||
| chr9:35732365-35732676 | Common:2; Rare:79 | ||||
| chr9:35748993-35749354 | Common:2; Rare:136 | ||||
| chr9:35814983-35815293 | Rare:79 | ||||
| chr9:36190725-36190978 | Common:1; Rare:83 | ||||
| chr9:36258436-36258580 | Common:2; Rare:30; Clinvar:1 | ||||
| chr9:36572772-36572941 | Rare:47 | ||||
| chr9:37592449-37592648 | Common:3; Rare:75 | ||||
| chr9:37784996-37785109 | Common:1; Rare:66; Clinvar:1; Clinvar (benign):3 | ||||
| chr9:37800677-37800806 | Common:1; Rare:36 | ||||
| chr9:37904079-37904463 | Common:3; Rare:124 |