| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:99906570-99906762 | Rare:89 | ||||
| chr9:99906994-99907030 | Rare:7 | ||||
| chr9:99907042-99907115 | Rare:11 | ||||
| chr9:100098905-100099342 | Common:4; Rare:123; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:100352675-100353103 | Rare:146 | ||||
| chr9:101398503-101399111 | Common:1; Rare:181 | ||||
| chr9:101487043-101487088 | Rare:18 | ||||
| chr9:101487092-101487118 | Rare:6 | ||||
| chr9:101533654-101533999 | Common:3; Rare:101 | ||||
| chr9:101594851-101595039 | Rare:58 | ||||
| chr9:104093447-104093776 | Common:6; Rare:73 | ||||
| chr9:104093977-104094350 | Common:3; Rare:93 | ||||
| chr9:104094522-104094621 | Common:1; Rare:32 | ||||
| chr9:104747493-104747795 | Common:1; Rare:83 | ||||
| chr9:104747812-104747971 | Common:3; Rare:68 |