| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:124354919-124355002 | Rare:19 | ||||
| chr9:124355114-124355552 | Common:3; Rare:101 | ||||
| chr9:124356421-124356684 | Common:1; Rare:40 | ||||
| chr9:124357448-124358136 | Common:1; Rare:148 | ||||
| chr9:124362501-124362787 | Common:3; Rare:46 | ||||
| chr9:124658124-124658443 | Rare:59 | ||||
| chr9:125239062-125239530 | Rare:94 | ||||
| chr9:125538101-125538288 | Rare:29 | ||||
| chr9:127447974-127448059 | Rare:22 | ||||
| chr9:127450694-127450819 | Common:2; Rare:29 | ||||
| chr9:127543784-127543958 | Rare:37 | ||||
| chr9:127825814-127825933 | Common:1; Rare:32; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr9:127944613-127944915 | Common:1; Rare:108 | ||||
| chr9:127950015-127950085 | Rare:8 | ||||
| chr9:127952343-127952389 | Rare:14 |