| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:71911152-71911495 | Common:2; Rare:102 | ||||
| chr9:75088135-75088298 | Common:2; Rare:52 | ||||
| chr9:83707653-83707730 | Rare:30 | ||||
| chr9:83980153-83980554 | Common:1; Rare:146 | ||||
| chr9:83980581-83980716 | Common:3; Rare:52 | ||||
| chr9:91950149-91950355 | Common:2; Rare:56 | ||||
| chr9:93451483-93451889 | Common:3; Rare:120 | ||||
| chr9:97633329-97633825 | Common:6; Rare:154 | ||||
| chr9:99221898-99222329 | Common:2; Rare:166; Clinvar:2; Clinvar (benign):3 | ||||
| chr9:100098943-100099255 | Common:2; Rare:86 | ||||
| chr9:100352874-100353071 | Rare:66 | ||||
| chr9:107283327-107283634 | Common:3; Rare:69 | ||||
| chr9:108934116-108934421 | Common:6; Rare:110; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:110579076-110579299 | Rare:57 | ||||
| chr9:111483557-111483710 | Common:2; Rare:69 |