| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:50623876-50624070 | Common:1; Rare:73 | ||||
| chr10:50990867-50990945 | Common:2; Rare:13 | ||||
| chr10:51074364-51074520 | Rare:26 | ||||
| chr10:51699536-51699865 | Common:4; Rare:94 | ||||
| chr10:58268945-58269268 | Common:5; Rare:102 | ||||
| chr10:60300337-60300540 | Common:1; Rare:41 | ||||
| chr10:62049062-62049482 | Common:2; Rare:80 | ||||
| chr10:62816349-62816511 | Rare:28 | ||||
| chr10:63465963-63466306 | Common:4; Rare:133 | ||||
| chr10:68331914-68332164 | Common:1; Rare:105 | ||||
| chr10:68332884-68332999 | Common:1; Rare:29 | ||||
| chr10:68407252-68407361 | Common:3; Rare:30 | ||||
| chr10:68527422-68527585 | Common:2; Rare:59 | ||||
| chr10:68901049-68901365 | Common:3; Rare:124 | ||||
| chr10:68988488-68988835 | Common:1; Rare:76; Clinvar (benign):2 |