| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:43436794-43437143 | Common:4; Rare:150 | ||||
| chr10:43606360-43606507 | Common:3; Rare:50 | ||||
| chr10:43648800-43648975 | Common:1; Rare:50 | ||||
| chr10:44959558-44959815 | Common:2; Rare:80 | ||||
| chr10:45000745-45000961 | Common:1; Rare:93 | ||||
| chr10:45727162-45727311 | Common:1; Rare:66 | ||||
| chr10:45972352-45972582 | Common:1; Rare:75 | ||||
| chr10:46030530-46030746 | Common:1; Rare:68 | ||||
| chr10:48306422-48306741 | Common:2; Rare:132 | ||||
| chr10:49539014-49539217 | Common:3; Rare:69; Clinvar:2; Clinvar (benign):2 | ||||
| chr10:49941913-49942133 | Rare:68 | ||||
| chr10:50067862-50068013 | Common:3; Rare:69 | ||||
| chr10:50623897-50624084 | Common:1; Rare:78 | ||||
| chr10:50624631-50624984 | Common:5; Rare:119 | ||||
| chr10:50739905-50739983 | Rare:17 |