| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:39566317-39566469 | Common:1; Rare:74 | ||||
| chr7:39623492-39623825 | Rare:102 | ||||
| chr7:39949498-39949693 | Common:1; Rare:72 | ||||
| chr7:40134229-40134536 | Rare:125; Clinvar (pathogenic):1 | ||||
| chr7:40134539-40135101 | Common:1; Rare:175; Clinvar:1; Clinvar (benign):1 | ||||
| chr7:41700491-41700663 | Rare:26 | ||||
| chr7:41703004-41703382 | Common:2; Rare:64 | ||||
| chr7:42932151-42932494 | Rare:133 | ||||
| chr7:43583059-43583305 | Common:1; Rare:100 | ||||
| chr7:43583346-43583727 | Common:2; Rare:90 | ||||
| chr7:43622190-43622395 | Common:2; Rare:30 | ||||
| chr7:43648832-43649197 | Common:2; Rare:67 | ||||
| chr7:43649683-43649957 | Common:1; Rare:50 | ||||
| chr7:43650114-43650177 | Common:1; Rare:9 | ||||
| chr7:43729443-43729575 | Common:1; Rare:43 |