| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7687471-7687556 | Rare:20 | ||||
| chr17:7843672-7843745 | Rare:26 | ||||
| chr17:7857074-7857285 | Common:2; Rare:99 | ||||
| chr17:7857467-7858079 | Common:4; Rare:196 | ||||
| chr17:7858156-7858316 | Common:2; Rare:53 | ||||
| chr17:7885207-7885355 | Rare:48 | ||||
| chr17:7931890-7932268 | Common:5; Rare:104 | ||||
| chr17:8147544-8147772 | Common:1; Rare:83 | ||||
| chr17:8152378-8152629 | Common:2; Rare:60 | ||||
| chr17:8156561-8156869 | Common:3; Rare:86 | ||||
| chr17:8162878-8163093 | Common:1; Rare:77 | ||||
| chr17:8176313-8176441 | Rare:44 | ||||
| chr17:8189292-8189487 | Common:1; Rare:69 | ||||
| chr17:8248036-8248119 | Common:2; Rare:43; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:8249024-8249319 | Common:1; Rare:64 |