| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:27242025-27242414 | Common:2; Rare:143 | ||||
| chr10:27504027-27504374 | Rare:153; Clinvar:4; Clinvar (benign):1 | ||||
| chr10:27998800-27999020 | Common:1; Rare:62 | ||||
| chr10:28531859-28532548 | Common:10; Rare:239 | ||||
| chr10:28532614-28532821 | Common:1; Rare:89 | ||||
| chr10:28532962-28533141 | Rare:60 | ||||
| chr10:28677334-28677579 | Common:4; Rare:114 | ||||
| chr10:29522913-29523353 | Common:6; Rare:146 | ||||
| chr10:29735400-29735577 | Rare:86 | ||||
| chr10:29735889-29736222 | Common:2; Rare:74 | ||||
| chr10:29736276-29736935 | Common:4; Rare:166 | ||||
| chr10:30059490-30059790 | Common:2; Rare:93 | ||||
| chr10:30115023-30115717 | Common:4; Rare:176 | ||||
| chr10:30433373-30433486 | Rare:36 | ||||
| chr10:30433757-30434186 | Common:4; Rare:122 |