| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:47846729-47847129 | Common:5; Rare:139 | ||||
| chr17:47949200-47949580 | Common:1; Rare:85; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:47990924-47991074 | Rare:24 | ||||
| chr17:47991051-47991845 | Common:2; Rare:222 | ||||
| chr17:47995120-47995493 | Common:3; Rare:58 | ||||
| chr17:48002909-48003315 | Common:4; Rare:148 | ||||
| chr17:48003360-48003640 | Common:2; Rare:68 | ||||
| chr17:48003843-48004102 | Common:1; Rare:46 | ||||
| chr17:48004990-48005166 | Rare:32 | ||||
| chr17:48011470-48011623 | Common:5; Rare:58 | ||||
| chr17:48011896-48012172 | Rare:47 | ||||
| chr17:48012322-48012653 | Common:3; Rare:61 | ||||
| chr17:48012770-48013752 | Common:2; Rare:196 | ||||
| chr17:48013881-48014387 | Common:2; Rare:86 | ||||
| chr17:48014761-48015651 | Common:10; Rare:227 |