| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:26216251-26216487 | Common:1; Rare:55 | ||||
| chr10:26216620-26216817 | Common:1; Rare:51 | ||||
| chr10:26734348-26734652 | Common:2; Rare:65 | ||||
| chr10:27100427-27100603 | Common:3; Rare:51; Clinvar:4; Clinvar (benign):2 | ||||
| chr10:27154315-27154480 | Rare:43 | ||||
| chr10:27155227-27155439 | Common:6; Rare:95; Clinvar:2; Clinvar (benign):6 | ||||
| chr10:27240466-27240896 | Common:2; Rare:124 | ||||
| chr10:27242058-27242241 | Common:1; Rare:78 | ||||
| chr10:28532474-28532896 | Common:5; Rare:161 | ||||
| chr10:28533325-28533541 | Common:1; Rare:80 | ||||
| chr10:28677269-28677531 | Common:6; Rare:125 | ||||
| chr10:29735787-29736016 | Common:3; Rare:45 | ||||
| chr10:30059508-30059689 | Common:1; Rare:70 | ||||
| chr10:30349271-30349399 | Common:12; Rare:77 | ||||
| chr10:31031820-31032060 | Common:2; Rare:94 |