| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:28552582-28552755 | Rare:59; Clinvar:3; Clinvar (benign):1 | ||||
| chr17:28571492-28571716 | Rare:57 | ||||
| chr17:28576862-28577054 | Common:2; Rare:53 | ||||
| chr17:28598885-28599168 | Common:3; Rare:91 | ||||
| chr17:28645094-28645350 | Common:1; Rare:99 | ||||
| chr17:28661868-28661964 | Rare:42 | ||||
| chr17:28662166-28662327 | Rare:63 | ||||
| chr17:28711282-28711568 | Common:3; Rare:84 | ||||
| chr17:28717707-28718049 | Rare:69 | ||||
| chr17:28718136-28718208 | Rare:17 | ||||
| chr17:28719518-28720083 | Common:1; Rare:163 | ||||
| chr17:28720130-28720428 | Common:4; Rare:140 | ||||
| chr17:28727924-28728041 | Rare:28 | ||||
| chr17:28728643-28728790 | Rare:53 | ||||
| chr17:28812257-28812696 | Common:1; Rare:121 |