| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:49538967-49539227 | Common:3; Rare:92; Clinvar:3; Clinvar (benign):3 | ||||
| chr10:49941915-49942124 | Rare:64 | ||||
| chr10:50067837-50068004 | Common:4; Rare:79 | ||||
| chr10:50418084-50418198 | Common:1; Rare:31 | ||||
| chr10:50623872-50624092 | Common:1; Rare:85 | ||||
| chr10:50624852-50625058 | Common:2; Rare:66 | ||||
| chr10:50625168-50625262 | Common:1; Rare:27 | ||||
| chr10:50739910-50739988 | Rare:18 | ||||
| chr10:51699537-51699976 | Common:7; Rare:124 | ||||
| chr10:52314121-52314284 | Common:1; Rare:39 | ||||
| chr10:55627469-55627657 | Common:2; Rare:33 | ||||
| chr10:55628234-55628344 | Common:2; Rare:24 | ||||
| chr10:55628441-55628728 | Rare:63 | ||||
| chr10:56361228-56361518 | Common:6; Rare:103 | ||||
| chr10:58268937-58269288 | Common:6; Rare:113 |