| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:99821737-99822031 | Rare:74 | ||||
| chr9:99822183-99822285 | Rare:26 | ||||
| chr9:99906570-99906721 | Rare:69 | ||||
| chr9:100098970-100099350 | Common:4; Rare:108; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:100352858-100353089 | Rare:83 | ||||
| chr9:100427115-100427384 | Common:3; Rare:95 | ||||
| chr9:101398570-101398910 | Common:1; Rare:114 | ||||
| chr9:101487050-101487185 | Common:1; Rare:41 | ||||
| chr9:101533684-101533907 | Common:1; Rare:70 | ||||
| chr9:104093985-104094321 | Common:3; Rare:78 | ||||
| chr9:104747608-104747799 | Common:1; Rare:59 | ||||
| chr9:105557860-105558170 | Rare:77; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:105694481-105694623 | Common:2; Rare:66 | ||||
| chr9:106862950-106863180 | Rare:75 | ||||
| chr9:106863527-106863660 | Rare:23 |