| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:44384961-44385208 | Common:1; Rare:110 | ||||
| chr10:44959707-44959830 | Common:1; Rare:45 | ||||
| chr10:45000766-45000968 | Common:1; Rare:86 | ||||
| chr10:45373989-45374292 | Common:5; Rare:105 | ||||
| chr10:45726945-45727307 | Common:6; Rare:114 | ||||
| chr10:45972343-45972577 | Common:1; Rare:75 | ||||
| chr10:46030541-46030739 | Common:1; Rare:64 | ||||
| chr10:49115466-49115625 | Rare:53 | ||||
| chr10:49539023-49539175 | Common:2; Rare:48; Clinvar:2; Clinvar (benign):2 | ||||
| chr10:49941922-49942124 | Rare:60 | ||||
| chr10:50067659-50068008 | Common:6; Rare:125 | ||||
| chr10:50623881-50624079 | Common:1; Rare:79 | ||||
| chr10:50624861-50624976 | Common:1; Rare:45 | ||||
| chr10:50739905-50739970 | Rare:14 | ||||
| chr10:50991201-50991385 | Common:4; Rare:55 |