| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:92325316-92325988 | Common:9; Rare:183 | ||||
| chr9:92404530-92404664 | Rare:33 | ||||
| chr9:92482336-92482424 | Rare:13 | ||||
| chr9:92482459-92482568 | Rare:14 | ||||
| chr9:92535978-92536187 | Common:1; Rare:29 | ||||
| chr9:92536611-92536790 | Common:2; Rare:21 | ||||
| chr9:92670002-92670326 | Common:1; Rare:101 | ||||
| chr9:92764787-92765120 | Common:2; Rare:104; Clinvar (benign):1 | ||||
| chr9:93451455-93451694 | Common:3; Rare:67 | ||||
| chr9:93452267-93452330 | Rare:10 | ||||
| chr9:93452336-93452387 | Rare:10 | ||||
| chr9:93452919-93452940 | Rare:7 | ||||
| chr9:93453546-93453696 | Rare:34 | ||||
| chr9:94639420-94639587 | Common:1; Rare:47; Clinvar:6; Clinvar (benign):1 | ||||
| chr9:94640233-94640444 | Common:2; Rare:36 |