| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:97666575-97666815 | Common:1; Rare:41 | ||||
| chr9:97697268-97697436 | Common:1; Rare:102; Clinvar:5; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr9:97922171-97922225 | Rare:20 | ||||
| chr9:97922384-97922622 | Common:5; Rare:111 | ||||
| chr9:97983217-97983603 | Common:2; Rare:144 | ||||
| chr9:97984506-97984570 | Rare:29 | ||||
| chr9:98056550-98056810 | Common:2; Rare:94 | ||||
| chr9:98192605-98192852 | Common:5; Rare:68 | ||||
| chr9:98255593-98256057 | Common:3; Rare:124 | ||||
| chr9:98555870-98555998 | Rare:15 | ||||
| chr9:98943545-98943585 | Rare:2 | ||||
| chr9:98943824-98943993 | Common:1; Rare:61 | ||||
| chr9:99104806-99105054 | Common:2; Rare:71 | ||||
| chr9:99221540-99221678 | Rare:57; Clinvar:2; Clinvar (benign):3 | ||||
| chr9:99221892-99222364 | Common:2; Rare:190; Clinvar:3; Clinvar (benign):3 |