| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:97445969-97446229 | Common:1; Rare:69 | ||||
| chr10:97498387-97498544 | Common:2; Rare:62 | ||||
| chr10:97633435-97633662 | Common:2; Rare:60 | ||||
| chr10:97736936-97737198 | Common:2; Rare:90 | ||||
| chr10:98134537-98134688 | Common:1; Rare:54 | ||||
| chr10:99430616-99430930 | Common:3; Rare:70 | ||||
| chr10:99659247-99659547 | Common:1; Rare:77 | ||||
| chr10:99732088-99732355 | Rare:95; Clinvar:3 | ||||
| chr10:100185914-100186105 | Rare:78 | ||||
| chr10:100346942-100347252 | Common:1; Rare:77 | ||||
| chr10:100529847-100529968 | Rare:33 | ||||
| chr10:100912655-100913005 | Common:1; Rare:102 | ||||
| chr10:100913335-100913359 | Rare:8 | ||||
| chr10:100969378-100969552 | Common:2; Rare:34 | ||||
| chr10:100987445-100987593 | Common:1; Rare:56; Clinvar:1; Clinvar (benign):1 |