| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:28406137-28406268 | Rare:23; Clinvar:1 | ||||
| chr17:28552585-28552739 | Rare:52; Clinvar:3; Clinvar (benign):1 | ||||
| chr17:28571497-28571664 | Rare:39 | ||||
| chr17:28598965-28599170 | Common:2; Rare:67 | ||||
| chr17:28661876-28661964 | Rare:38 | ||||
| chr17:28662122-28662319 | Rare:79 | ||||
| chr17:28727970-28728041 | Rare:13 | ||||
| chr17:28728694-28728806 | Rare:43 | ||||
| chr17:28812410-28812669 | Common:1; Rare:65 | ||||
| chr17:28842709-28842856 | Common:1; Rare:56 | ||||
| chr17:28854988-28855032 | Rare:12 | ||||
| chr17:28897025-28897243 | Rare:53 | ||||
| chr17:28897584-28897758 | Common:1; Rare:57 | ||||
| chr17:29042619-29042822 | Common:2; Rare:47 | ||||
| chr17:29140379-29140460 | Common:2; Rare:27 |