| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:58218583-58218691 | Rare:29; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr17:58219110-58219468 | Common:2; Rare:136; Clinvar:7; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr17:58352116-58352499 | Common:6; Rare:142 | ||||
| chr17:58352549-58352592 | Common:1; Rare:9 | ||||
| chr17:58353029-58353170 | Common:1; Rare:26 | ||||
| chr17:58513984-58514410 | Rare:84 | ||||
| chr17:58514415-58514433 | Rare:4 | ||||
| chr17:58514548-58514796 | Rare:58 | ||||
| chr17:58517783-58517945 | Common:1; Rare:34 | ||||
| chr17:58517997-58518297 | Rare:68 | ||||
| chr17:58692495-58692803 | Common:3; Rare:159; Clinvar:36; Clinvar (benign):33; Clinvar (pathogenic):3 | ||||
| chr17:58692820-58692948 | Common:1; Rare:38 | ||||
| chr17:58693067-58693385 | Common:1; Rare:74 | ||||
| chr17:58755786-58755885 | Rare:22 | ||||
| chr17:59106264-59106466 | Common:1; Rare:57 |