| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:26199964-26200014 | Rare:19 | ||||
| chr7:30410412-30410621 | Common:2; Rare:40 | ||||
| chr7:30507459-30507719 | Common:2; Rare:41 | ||||
| chr7:32728079-32728139 | Common:1; Rare:22 | ||||
| chr7:32942458-32942645 | Common:1; Rare:50 | ||||
| chr7:39733525-39733626 | Rare:17 | ||||
| chr7:43643146-43643176 | Rare:8 | ||||
| chr7:44038923-44039196 | Common:5; Rare:49 | ||||
| chr7:44107915-44108103 | Common:2; Rare:62; Clinvar (pathogenic):1 | ||||
| chr7:44467729-44467888 | Common:3; Rare:35 | ||||
| chr7:44581213-44581287 | Common:2; Rare:19 | ||||
| chr7:44618809-44619102 | Common:2; Rare:54 | ||||
| chr7:44986574-44986793 | Common:4; Rare:104 | ||||
| chr7:45768930-45769158 | Common:2; Rare:72 | ||||
| chr7:51076027-51076069 | Rare:6 |