| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:44978798-44978970 | Common:3; Rare:50 | ||||
| chr10:45000766-45000968 | Common:1; Rare:86 | ||||
| chr10:45727129-45727320 | Common:1; Rare:77 | ||||
| chr10:45972343-45972572 | Common:1; Rare:72 | ||||
| chr10:46030541-46030758 | Common:1; Rare:69 | ||||
| chr10:48306386-48306754 | Common:2; Rare:146 | ||||
| chr10:48605047-48605155 | Common:1; Rare:30 | ||||
| chr10:49539007-49539175 | Common:2; Rare:54; Clinvar:2; Clinvar (benign):2 | ||||
| chr10:49941913-49942134 | Rare:69 | ||||
| chr10:50067830-50068008 | Common:4; Rare:80 | ||||
| chr10:50623866-50624090 | Common:1; Rare:84 | ||||
| chr10:50624867-50624974 | Common:1; Rare:43 | ||||
| chr10:50739890-50739970 | Rare:17 | ||||
| chr10:51074402-51074674 | Common:1; Rare:63; Clinvar (benign):7 | ||||
| chr10:51699557-51699854 | Common:4; Rare:81 |