| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:45972352-45972582 | Common:1; Rare:75 | ||||
| chr10:46030547-46030758 | Common:1; Rare:69 | ||||
| chr10:46911326-46911467 | Rare:11 | ||||
| chr10:48306572-48306820 | Common:2; Rare:110 | ||||
| chr10:49539014-49539213 | Common:3; Rare:67; Clinvar:2; Clinvar (benign):2 | ||||
| chr10:49941913-49942139 | Rare:71 | ||||
| chr10:50067791-50067995 | Common:4; Rare:93 | ||||
| chr10:50623891-50624084 | Common:1; Rare:78 | ||||
| chr10:50624894-50624976 | Common:1; Rare:33 | ||||
| chr10:50739866-50739982 | Rare:24 | ||||
| chr10:51074029-51074353 | Common:5; Rare:77 | ||||
| chr10:51074382-51074674 | Common:1; Rare:69; Clinvar (benign):7 | ||||
| chr10:56361232-56361484 | Common:5; Rare:83 | ||||
| chr10:58268937-58269268 | Common:6; Rare:103 | ||||
| chr10:58385308-58385482 | Common:2; Rare:66 |