| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:36258395-36258599 | Common:2; Rare:49; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:37785021-37785155 | Common:1; Rare:59; Clinvar:1; Clinvar (benign):2 | ||||
| chr9:37800707-37800837 | Rare:40 | ||||
| chr9:37904076-37904219 | Rare:49 | ||||
| chr9:37904346-37904414 | Rare:22 | ||||
| chr9:38392500-38392795 | Common:2; Rare:78 | ||||
| chr9:66900479-66900804 | Common:4; Rare:99 | ||||
| chr9:68356808-68357125 | Common:5; Rare:81 | ||||
| chr9:69759907-69760147 | Common:3; Rare:103 | ||||
| chr9:70258845-70259069 | Common:3; Rare:106 | ||||
| chr9:70413903-70414201 | Rare:61 | ||||
| chr9:70414299-70414511 | Rare:51 | ||||
| chr9:71768850-71769039 | Common:2; Rare:58 | ||||
| chr9:71911187-71911499 | Common:2; Rare:90 | ||||
| chr9:73151696-73151921 | Rare:41 |