| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:35695008-35695277 | Common:2; Rare:85 | ||||
| chr7:35800981-35801255 | Common:1; Rare:117 | ||||
| chr7:37448790-37449165 | Common:1; Rare:107 | ||||
| chr7:39566234-39566410 | Common:1; Rare:77 | ||||
| chr7:39949349-39949693 | Common:2; Rare:126 | ||||
| chr7:39949944-39950272 | Common:1; Rare:102 | ||||
| chr7:39951619-39951839 | Rare:88; Clinvar (benign):1 | ||||
| chr7:40134588-40134663 | Rare:25 | ||||
| chr7:42932149-42932384 | Rare:86 | ||||
| chr7:43648752-43649039 | Common:1; Rare:55 | ||||
| chr7:43649990-43650121 | Rare:20 | ||||
| chr7:43869496-43869703 | Rare:55 | ||||
| chr7:43926355-43926457 | Rare:35 | ||||
| chr7:44044606-44044776 | Common:2; Rare:43 | ||||
| chr7:44116240-44116482 | Rare:67 |