| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:44708764-44708899 | Common:3; Rare:49 | ||||
| chr17:44846190-44846359 | Rare:20 | ||||
| chr17:44899375-44899799 | Common:3; Rare:130; Clinvar:3; Clinvar (benign):1 | ||||
| chr17:45051437-45051688 | Common:1; Rare:86 | ||||
| chr17:45060992-45061398 | Common:2; Rare:120 | ||||
| chr17:45132340-45132633 | Common:2; Rare:88 | ||||
| chr17:45148154-45148637 | Common:1; Rare:165 | ||||
| chr17:45148702-45148868 | Rare:49 | ||||
| chr17:45161481-45161637 | Rare:44 | ||||
| chr17:45245127-45245313 | Common:1; Rare:50 | ||||
| chr17:45431913-45432026 | Common:2; Rare:18 | ||||
| chr17:45490688-45490893 | Common:1; Rare:68 | ||||
| chr17:45620218-45620367 | Rare:37 | ||||
| chr17:46192801-46193007 | Common:2; Rare:48; Clinvar (benign):1 | ||||
| chr17:46193381-46193604 | Common:3; Rare:59 |