| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:40219168-40219436 | Common:6; Rare:184 | ||||
| chr17:40219500-40219860 | Common:2; Rare:106 | ||||
| chr17:40287583-40288067 | Rare:117 | ||||
| chr17:40318061-40318297 | Common:2; Rare:97 | ||||
| chr17:40417806-40418204 | Rare:228 | ||||
| chr17:40501559-40501761 | Common:1; Rare:43 | ||||
| chr17:40818741-40819631 | Common:14; Rare:416; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr17:40821960-40822345 | Common:4; Rare:164; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr17:41521757-41522200 | Common:6; Rare:127 | ||||
| chr17:41528253-41528550 | Common:2; Rare:109; Clinvar:2 | ||||
| chr17:41612762-41612883 | Rare:18 | ||||
| chr17:41624251-41624493 | Rare:122 | ||||
| chr17:41624551-41624905 | Common:3; Rare:127 | ||||
| chr17:41688599-41688996 | Common:3; Rare:289 | ||||
| chr17:41689287-41689596 | Common:6; Rare:220 |