| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:19378162-19378537 | Common:2; Rare:92 | ||||
| chr17:19648536-19648851 | Common:4; Rare:101 | ||||
| chr17:19977804-19977974 | Common:1; Rare:58 | ||||
| chr17:21214123-21214344 | Common:2; Rare:99 | ||||
| chr17:27293910-27294132 | Common:1; Rare:91 | ||||
| chr17:28335371-28335850 | Common:1; Rare:113 | ||||
| chr17:28357455-28357692 | Common:5; Rare:121; Clinvar (pathogenic):1 | ||||
| chr17:28571492-28571663 | Rare:43 | ||||
| chr17:28599007-28599165 | Common:2; Rare:41 | ||||
| chr17:28645091-28645343 | Common:1; Rare:99 | ||||
| chr17:28661877-28661964 | Rare:37 | ||||
| chr17:28662166-28662303 | Rare:57 | ||||
| chr17:28717700-28718028 | Rare:66 | ||||
| chr17:28718130-28718236 | Rare:25 | ||||
| chr17:28812377-28812641 | Common:1; Rare:67 |