| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:57868235-57868292 | Common:1; Rare:21 | ||||
| chr17:57987919-57988077 | Common:3; Rare:57 | ||||
| chr17:57988107-57988535 | Common:6; Rare:122 | ||||
| chr17:58007205-58007384 | Common:1; Rare:77 | ||||
| chr17:58219184-58219385 | Common:1; Rare:81; Clinvar:5; Clinvar (benign):5 | ||||
| chr17:58352116-58352661 | Common:7; Rare:174 | ||||
| chr17:58417481-58417597 | Rare:24 | ||||
| chr17:58526968-58527034 | Rare:33 | ||||
| chr17:58529225-58529550 | Rare:50 | ||||
| chr17:58531962-58532150 | Rare:46 | ||||
| chr17:58539187-58539453 | Rare:39 | ||||
| chr17:58692528-58692706 | Common:1; Rare:92; Clinvar:21; Clinvar (benign):20 | ||||
| chr17:59106701-59107024 | Common:2; Rare:108; Clinvar:4; Clinvar (benign):2 | ||||
| chr17:59155143-59155552 | Common:2; Rare:96 | ||||
| chr17:59331491-59331803 | Common:2; Rare:102 |