| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:100185924-100186184 | Rare:101 | ||||
| chr10:100229566-100229652 | Rare:24 | ||||
| chr10:100267589-100267746 | Common:3; Rare:52 | ||||
| chr10:100286624-100286730 | Common:2; Rare:62 | ||||
| chr10:100346911-100347276 | Common:1; Rare:86 | ||||
| chr10:100529844-100529924 | Rare:27 | ||||
| chr10:100912737-100912996 | Common:1; Rare:80 | ||||
| chr10:100913328-100913355 | Rare:9 | ||||
| chr10:100987421-100987590 | Common:1; Rare:68; Clinvar:1; Clinvar (benign):1 | ||||
| chr10:101031102-101031264 | Common:1; Rare:39 | ||||
| chr10:101588263-101588329 | Rare:30 | ||||
| chr10:101818368-101818749 | Common:1; Rare:103 | ||||
| chr10:102056100-102056327 | Common:1; Rare:55 | ||||
| chr10:102114925-102115133 | Common:2; Rare:60 | ||||
| chr10:102152043-102152413 | Common:3; Rare:117 |