| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:37592459-37592682 | Common:2; Rare:76 | ||||
| chr9:37785028-37785309 | Common:1; Rare:99; Clinvar:1; Clinvar (benign):2 | ||||
| chr9:37800707-37800816 | Rare:30 | ||||
| chr9:37903702-37904237 | Common:3; Rare:165 | ||||
| chr9:38620577-38620773 | Rare:59 | ||||
| chr9:43127129-43127439 | Common:2; Rare:81 | ||||
| chr9:68779950-68780162 | Common:2; Rare:73 | ||||
| chr9:69173865-69174332 | Common:6; Rare:145 | ||||
| chr9:70168444-70168755 | Common:2; Rare:56 | ||||
| chr9:70258830-70259081 | Common:4; Rare:117 | ||||
| chr9:70414293-70414415 | Rare:21 | ||||
| chr9:71768431-71768622 | Rare:46 | ||||
| chr9:71768840-71769036 | Common:2; Rare:59 | ||||
| chr9:71911165-71911499 | Common:2; Rare:98 | ||||
| chr9:71911617-71911731 | Common:1; Rare:37 |