| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:124415365-124415608 | Common:1; Rare:89 | ||||
| chr9:124861786-124862157 | Common:1; Rare:148 | ||||
| chr9:124862304-124862430 | Common:1; Rare:29 | ||||
| chr9:124872400-124872621 | Common:3; Rare:48 | ||||
| chr9:124940949-124941202 | Common:3; Rare:99 | ||||
| chr9:125189725-125190039 | Common:1; Rare:142 | ||||
| chr9:125200287-125200596 | Common:1; Rare:106 | ||||
| chr9:125241006-125241713 | Common:6; Rare:231 | ||||
| chr9:125261712-125261854 | Common:1; Rare:49 | ||||
| chr9:125707132-125707381 | Common:2; Rare:81 | ||||
| chr9:126804912-126805064 | Common:1; Rare:51 | ||||
| chr9:127245188-127245341 | Common:1; Rare:37 | ||||
| chr9:127424034-127424488 | Common:1; Rare:138 | ||||
| chr9:127449279-127449737 | Common:2; Rare:125 | ||||
| chr9:127451049-127451565 | Common:5; Rare:199; Clinvar (benign):1 |