| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:49134012-49134120 | Common:3; Rare:28 | ||||
| chr10:49539001-49539136 | Common:2; Rare:43; Clinvar:2; Clinvar (benign):2 | ||||
| chr10:49679577-49679719 | Common:1; Rare:51 | ||||
| chr10:49941908-49942139 | Rare:74 | ||||
| chr10:49988192-49988412 | Common:1; Rare:27 | ||||
| chr10:50067837-50068013 | Common:4; Rare:80 | ||||
| chr10:50623372-50623520 | Common:2; Rare:29 | ||||
| chr10:50623872-50624084 | Common:1; Rare:84 | ||||
| chr10:50624510-50624548 | Rare:21 | ||||
| chr10:50624911-50624989 | Common:1; Rare:30 | ||||
| chr10:50625141-50625252 | Common:1; Rare:29 | ||||
| chr10:50739890-50739988 | Rare:23 | ||||
| chr10:50991085-50991385 | Common:4; Rare:80 | ||||
| chr10:51074382-51074575 | Common:1; Rare:44; Clinvar (benign):2 | ||||
| chr10:51699536-51699648 | Common:1; Rare:43 |