| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:100267616-100267763 | Common:2; Rare:44 | ||||
| chr10:100286605-100286730 | Common:4; Rare:73 | ||||
| chr10:100346921-100347531 | Common:4; Rare:145 | ||||
| chr10:100529770-100529991 | Common:1; Rare:67 | ||||
| chr10:100535747-100535961 | Common:6; Rare:78 | ||||
| chr10:100912741-100913047 | Common:1; Rare:94 | ||||
| chr10:100987180-100987604 | Common:1; Rare:153; Clinvar:1; Clinvar (benign):1 | ||||
| chr10:100996990-100997132 | Rare:41 | ||||
| chr10:100998525-100998716 | Common:2; Rare:36 | ||||
| chr10:101031102-101031485 | Common:1; Rare:88 | ||||
| chr10:101588140-101588336 | Rare:80 | ||||
| chr10:101783362-101783466 | Rare:51 | ||||
| chr10:101818083-101818190 | Rare:36 | ||||
| chr10:101818350-101818778 | Common:1; Rare:115 | ||||
| chr10:102056091-102056377 | Common:1; Rare:71 |