| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:100267589-100267763 | Common:3; Rare:56 | ||||
| chr10:100286603-100286735 | Common:5; Rare:79 | ||||
| chr10:100346911-100347438 | Common:3; Rare:119 | ||||
| chr10:100529794-100529991 | Common:1; Rare:61 | ||||
| chr10:100535796-100535970 | Common:6; Rare:74 | ||||
| chr10:100912737-100913062 | Common:1; Rare:98 | ||||
| chr10:100913325-100913406 | Rare:25 | ||||
| chr10:100987090-100987613 | Common:2; Rare:189; Clinvar:1; Clinvar (benign):2 | ||||
| chr10:100996969-100997144 | Common:2; Rare:47 | ||||
| chr10:101031093-101031302 | Common:1; Rare:48 | ||||
| chr10:101061749-101061999 | Rare:38 | ||||
| chr10:101588126-101588348 | Rare:95; Clinvar:1 | ||||
| chr10:101694896-101695242 | Rare:81; Clinvar:2 | ||||
| chr10:101783271-101783489 | Rare:98 | ||||
| chr10:101818136-101818228 | Rare:32 |