| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:30906480-30906696 | Rare:29 | ||||
| chr17:30921838-30922006 | Common:1; Rare:44 | ||||
| chr17:31094525-31094614 | Rare:24 | ||||
| chr17:31094701-31095038 | Common:2; Rare:84; Clinvar:1 | ||||
| chr17:31095321-31095609 | Rare:73; Clinvar:2; Clinvar (benign):5 | ||||
| chr17:31391555-31391689 | Rare:28 | ||||
| chr17:31487595-31488162 | Common:1; Rare:172 | ||||
| chr17:31488213-31488276 | Rare:16 | ||||
| chr17:31488455-31488509 | Rare:13 | ||||
| chr17:31858804-31858855 | Rare:17 | ||||
| chr17:31859147-31859476 | Common:3; Rare:85 | ||||
| chr17:31901546-31902000 | Common:4; Rare:139 | ||||
| chr17:31936704-31937229 | Common:2; Rare:158 | ||||
| chr17:31937238-31937400 | Rare:51 | ||||
| chr17:31937459-31937528 | Rare:14 |