| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:4788811-4789112 | Rare:169 | ||||
| chr17:4806961-4807210 | Common:8; Rare:154 | ||||
| chr17:4833109-4833530 | Common:1; Rare:207 | ||||
| chr17:4833730-4834060 | Common:1; Rare:65 | ||||
| chr17:4939902-4940394 | Common:4; Rare:274 | ||||
| chr17:4948308-4948739 | Common:9; Rare:304 | ||||
| chr17:4948888-4949194 | Common:3; Rare:156 | ||||
| chr17:4949280-4949702 | Common:3; Rare:181 | ||||
| chr17:4949809-4950218 | Common:2; Rare:183 | ||||
| chr17:4950801-4951123 | Common:1; Rare:75; Clinvar (benign):1 | ||||
| chr17:4967247-4967636 | Common:4; Rare:164 | ||||
| chr17:4967787-4967922 | Rare:94 | ||||
| chr17:4969023-4969214 | Common:1; Rare:61 | ||||
| chr17:4986458-4986890 | Common:4; Rare:154 | ||||
| chr17:4987317-4987831 | Common:8; Rare:285 |