| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:54968474-54968814 | Common:3; Rare:132 | ||||
| chr17:55265788-55265851 | Rare:14 | ||||
| chr17:55265865-55265885 | Rare:4 | ||||
| chr17:55266154-55266308 | Common:2; Rare:35 | ||||
| chr17:55421753-55422207 | Common:3; Rare:147 | ||||
| chr17:56833907-56834231 | Common:3; Rare:110 | ||||
| chr17:56914000-56914186 | Common:1; Rare:51 | ||||
| chr17:56978014-56978213 | Common:3; Rare:93 | ||||
| chr17:57084956-57085346 | Common:1; Rare:129 | ||||
| chr17:57085649-57085767 | Rare:25 | ||||
| chr17:57849967-57850274 | Common:1; Rare:108 | ||||
| chr17:57988100-57988512 | Common:6; Rare:118 | ||||
| chr17:58007205-58007488 | Common:1; Rare:119 | ||||
| chr17:58219216-58219372 | Common:1; Rare:62; Clinvar:2; Clinvar (benign):4 | ||||
| chr17:58692549-58692668 | Common:1; Rare:67; Clinvar:10; Clinvar (benign):20 |