| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:63859628-63859696 | Common:1; Rare:4 | ||||
| chr9:65884836-65884976 | |||||
| chr9:69250790-69251088 | Common:3; Rare:51; Clinvar:1; Clinvar (benign):3 | ||||
| chr9:70413083-70413128 | Rare:6 | ||||
| chr9:70413406-70413675 | Rare:89 | ||||
| chr9:70470543-70470741 | Rare:30 | ||||
| chr9:72154886-72155065 | Common:1; Rare:39 | ||||
| chr9:83219231-83219345 | Common:2; Rare:30 | ||||
| chr9:89994182-89994419 | Rare:28 | ||||
| chr9:90992054-90992346 | Common:4; Rare:43 | ||||
| chr9:91000067-91000145 | Rare:18 | ||||
| chr9:91100638-91100746 | Common:3; Rare:20 | ||||
| chr9:91193734-91193840 | Common:3; Rare:31 | ||||
| chr9:91210361-91210602 | Common:2; Rare:44 | ||||
| chr9:92098094-92098362 | Common:3; Rare:61 |