| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:104763982-104764201 | Common:2; Rare:48 | ||||
| chr9:104764270-104764402 | Common:1; Rare:56 | ||||
| chr9:105447936-105448144 | Common:2; Rare:76 | ||||
| chr9:105558067-105558189 | Rare:36; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:105558298-105558588 | Common:1; Rare:61 | ||||
| chr9:105694430-105694651 | Common:3; Rare:103 | ||||
| chr9:105700830-105700969 | Rare:27 | ||||
| chr9:106862938-106863186 | Rare:80 | ||||
| chr9:106863514-106863665 | Common:1; Rare:26 | ||||
| chr9:106932523-106932648 | Rare:32 | ||||
| chr9:107283012-107283302 | Common:1; Rare:97 | ||||
| chr9:107284531-107284647 | Rare:21 | ||||
| chr9:107489848-107490175 | Common:4; Rare:127 | ||||
| chr9:107490237-107490259 | Rare:8 | ||||
| chr9:108862149-108862364 | Rare:44 |