| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:40991963-40992385 | Common:7; Rare:32 | ||||
| chr9:62897686-62897736 | Common:1; Rare:16 | ||||
| chr9:62898028-62898143 | Common:2; Rare:18 | ||||
| chr9:67724185-67724375 | Common:13; Rare:9 | ||||
| chr9:69099376-69099841 | Common:7; Rare:96 | ||||
| chr9:69171114-69171150 | Common:1; Rare:1 | ||||
| chr9:70413950-70414068 | Rare:20 | ||||
| chr9:83219210-83219351 | Common:2; Rare:36 | ||||
| chr9:87042049-87042204 | Rare:53 | ||||
| chr9:97687220-97687306 | Rare:22; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr9:106859928-106860207 | Common:1; Rare:71 | ||||
| chr9:111959753-111959860 | Rare:16 | ||||
| chr9:114397938-114398138 | Rare:41 | ||||
| chr9:124658265-124658436 | Rare:33 | ||||
| chr9:131373447-131373679 | Common:1; Rare:57 |