| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:1684794-1685064 | Common:2; Rare:88; Clinvar:4; Clinvar (benign):1 | ||||
| chr17:1716204-1716562 | Common:4; Rare:115 | ||||
| chr17:1829770-1830082 | Common:8; Rare:133 | ||||
| chr17:2303461-2303650 | Rare:69 | ||||
| chr17:2303716-2304001 | Common:2; Rare:109 | ||||
| chr17:2330361-2330587 | Common:3; Rare:53 | ||||
| chr17:2336423-2336563 | Rare:53 | ||||
| chr17:2401616-2401718 | Rare:43 | ||||
| chr17:2511766-2512028 | Common:2; Rare:76 | ||||
| chr17:2593464-2593664 | Common:2; Rare:77 | ||||
| chr17:2593863-2593998 | Common:1; Rare:34; Clinvar:1; Clinvar (benign):3 | ||||
| chr17:2711762-2712043 | Common:2; Rare:79 | ||||
| chr17:3636241-3636511 | Common:4; Rare:76; Clinvar (benign):1 | ||||
| chr17:3636617-3636779 | Common:1; Rare:42; Clinvar:3; Clinvar (benign):1 | ||||
| chr17:3668533-3668876 | Common:3; Rare:139 |