| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:714799-714963 | Common:2; Rare:54 | ||||
| chr17:752146-752426 | Common:3; Rare:112 | ||||
| chr17:1400062-1400358 | Common:3; Rare:123 | ||||
| chr17:1516596-1516960 | Common:1; Rare:126 | ||||
| chr17:1684802-1685038 | Common:2; Rare:77; Clinvar:3; Clinvar (benign):1 | ||||
| chr17:1829801-1830071 | Common:7; Rare:113 | ||||
| chr17:2303728-2303968 | Common:2; Rare:88 | ||||
| chr17:2336415-2336572 | Rare:66 | ||||
| chr17:2511806-2512021 | Common:2; Rare:68 | ||||
| chr17:2593817-2593970 | Common:1; Rare:43; Clinvar:3; Clinvar (benign):3 | ||||
| chr17:3636241-3636503 | Common:4; Rare:74; Clinvar (benign):1 | ||||
| chr17:3668571-3668824 | Common:1; Rare:98 | ||||
| chr17:3723749-3723947 | Common:1; Rare:115 | ||||
| chr17:4142985-4143218 | Rare:83 | ||||
| chr17:4143638-4143740 | Common:3; Rare:54 |