| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:15478533-15478813 | Common:3; Rare:84 | ||||
| chr9:15479616-15479839 | Common:1; Rare:70 | ||||
| chr9:27047193-27047361 | Common:2; Rare:50 | ||||
| chr9:27497998-27498115 | Rare:32 | ||||
| chr9:27529037-27529153 | Rare:24 | ||||
| chr9:32550829-32551183 | Common:1; Rare:139; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:33446412-33446608 | Common:2; Rare:34 | ||||
| chr9:33816459-33816570 | Common:1; Rare:12 | ||||
| chr9:33818707-33818944 | Common:1; Rare:48 | ||||
| chr9:33916809-33917054 | Common:1; Rare:60 | ||||
| chr9:34551950-34552295 | Common:2; Rare:101 | ||||
| chr9:35067935-35068292 | Common:2; Rare:71; Clinvar (benign):2 | ||||
| chr9:35114087-35114390 | Rare:68 | ||||
| chr9:35604014-35604212 | Common:3; Rare:56 | ||||
| chr9:35617136-35617361 | Rare:52 |