| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:101031102-101031275 | Common:1; Rare:41 | ||||
| chr10:101588140-101588338 | Rare:81 | ||||
| chr10:101694846-101695273 | Common:1; Rare:95; Clinvar:2; Clinvar (benign):1 | ||||
| chr10:101818342-101818778 | Common:1; Rare:118 | ||||
| chr10:102056089-102056359 | Common:1; Rare:65 | ||||
| chr10:102114943-102115061 | Common:1; Rare:41 | ||||
| chr10:102394315-102394570 | Rare:71 | ||||
| chr10:102395558-102395722 | Common:1; Rare:45 | ||||
| chr10:102420523-102420866 | Rare:64 | ||||
| chr10:102421013-102421247 | Rare:103 | ||||
| chr10:102432525-102432835 | Common:2; Rare:92 | ||||
| chr10:102502617-102502904 | Common:1; Rare:85 | ||||
| chr10:102644988-102645163 | Rare:38 | ||||
| chr10:102714201-102714639 | Common:2; Rare:145 | ||||
| chr10:102776041-102776279 | Common:1; Rare:38 |