| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:56174069-56174220 | Rare:28 | ||||
| chr17:56174659-56174858 | Rare:31 | ||||
| chr17:56833178-56833532 | Common:1; Rare:105 | ||||
| chr17:56833783-56834221 | Common:5; Rare:131 | ||||
| chr17:56834479-56834504 | Common:1; Rare:4 | ||||
| chr17:56834835-56834977 | Common:1; Rare:58; Clinvar (pathogenic):1 | ||||
| chr17:56913388-56913725 | Common:2; Rare:103 | ||||
| chr17:56913757-56913848 | Rare:27 | ||||
| chr17:56913973-56914382 | Common:2; Rare:103 | ||||
| chr17:56960665-56960867 | Common:1; Rare:78 | ||||
| chr17:56960891-56961185 | Common:3; Rare:94 | ||||
| chr17:56978023-56978244 | Common:3; Rare:99 | ||||
| chr17:57084890-57085355 | Common:1; Rare:146 | ||||
| chr17:57085533-57086278 | Common:3; Rare:187 | ||||
| chr17:57086498-57086561 | Rare:16 |