| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:100536095-100536314 | Common:1; Rare:41 | ||||
| chr10:100912675-100913050 | Common:1; Rare:109 | ||||
| chr10:100913335-100913356 | Rare:7 | ||||
| chr10:100987436-100987599 | Common:1; Rare:64; Clinvar:1; Clinvar (benign):1 | ||||
| chr10:100996963-100997138 | Common:1; Rare:49 | ||||
| chr10:100998100-100998332 | Common:1; Rare:58 | ||||
| chr10:100999618-100999924 | Common:2; Rare:93 | ||||
| chr10:101031136-101031275 | Rare:33 | ||||
| chr10:101354015-101354193 | Common:1; Rare:75 | ||||
| chr10:101588166-101588339 | Rare:72 | ||||
| chr10:101694873-101695170 | Common:1; Rare:72; Clinvar:2; Clinvar (benign):1 | ||||
| chr10:101818618-101818798 | Common:1; Rare:44 | ||||
| chr10:101843591-101843675 | Common:1; Rare:20 | ||||
| chr10:101843815-101844137 | Common:3; Rare:107 | ||||
| chr10:102056089-102056351 | Common:1; Rare:61 |