| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:89923171-89923410 | Rare:103 | ||||
| chr16:89972462-89972621 | Common:1; Rare:54 | ||||
| chr17:410631-410646 | Rare:4 | ||||
| chr17:714626-714909 | Common:4; Rare:97; Clinvar (benign):3 | ||||
| chr17:732336-732633 | Common:2; Rare:103 | ||||
| chr17:752143-752339 | Common:2; Rare:77 | ||||
| chr17:752791-752902 | Rare:25 | ||||
| chr17:979321-979499 | Common:1; Rare:45 | ||||
| chr17:979653-980143 | Common:5; Rare:191 | ||||
| chr17:997355-997377 | Rare:7 | ||||
| chr17:1456105-1456483 | Common:4; Rare:149 | ||||
| chr17:1478410-1478734 | Common:1; Rare:125; Clinvar (benign):1 | ||||
| chr17:1485967-1486292 | Common:1; Rare:82 | ||||
| chr17:1491196-1491296 | Common:1; Rare:27 | ||||
| chr17:1491608-1491821 | Common:1; Rare:65 |