| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:58353032-58353194 | Common:1; Rare:32 | ||||
| chr17:58514002-58514116 | Rare:21 | ||||
| chr17:58514576-58514726 | Rare:30 | ||||
| chr17:58517766-58517916 | Common:1; Rare:48 | ||||
| chr17:58518057-58518359 | Rare:66 | ||||
| chr17:58692559-58692668 | Common:1; Rare:62; Clinvar:10; Clinvar (benign):20 | ||||
| chr17:58692820-58693160 | Common:1; Rare:88 | ||||
| chr17:58755576-58755904 | Common:1; Rare:69 | ||||
| chr17:59106692-59107146 | Common:2; Rare:152; Clinvar:4; Clinvar (benign):3 | ||||
| chr17:59155116-59155340 | Common:1; Rare:63 | ||||
| chr17:59155555-59155835 | Rare:70 | ||||
| chr17:59209924-59210089 | Rare:62 | ||||
| chr17:59220324-59220619 | Common:4; Rare:84 | ||||
| chr17:59331410-59331730 | Common:2; Rare:98 | ||||
| chr17:59565469-59565655 | Common:1; Rare:69 |