| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:1650043-1650165 | Rare:33 | ||||
| chr17:1684395-1684617 | Common:1; Rare:84; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:1684678-1685085 | Common:3; Rare:138; Clinvar:7; Clinvar (benign):1 | ||||
| chr17:1710300-1710535 | Rare:61 | ||||
| chr17:1710603-1710737 | Rare:30 | ||||
| chr17:1716092-1716892 | Common:5; Rare:235 | ||||
| chr17:1716974-1717368 | Common:2; Rare:85 | ||||
| chr17:1724549-1724782 | Common:2; Rare:86 | ||||
| chr17:1725058-1725129 | Rare:17 | ||||
| chr17:1725271-1725470 | Rare:62 | ||||
| chr17:1731050-1731239 | Rare:66; Clinvar (pathogenic):1 | ||||
| chr17:1770242-1770377 | Common:1; Rare:28 | ||||
| chr17:1829723-1830049 | Common:8; Rare:131 | ||||
| chr17:2024844-2024865 | Rare:5 | ||||
| chr17:2025099-2025128 | Rare:5 |