| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:27100427-27100619 | Common:3; Rare:56; Clinvar:4; Clinvar (benign):2 | ||||
| chr10:27154310-27154493 | Rare:50 | ||||
| chr10:27155165-27155453 | Common:7; Rare:119; Clinvar:5; Clinvar (benign):7 | ||||
| chr10:27240474-27240557 | Rare:37 | ||||
| chr10:27240565-27240601 | Rare:4 | ||||
| chr10:27240721-27240889 | Rare:46 | ||||
| chr10:27242058-27242235 | Common:1; Rare:76 | ||||
| chr10:28532715-28532927 | Common:1; Rare:73 | ||||
| chr10:28533032-28533230 | Rare:80 | ||||
| chr10:29486148-29486515 | Rare:100 | ||||
| chr10:29735768-29736016 | Common:3; Rare:47 | ||||
| chr10:29736880-29737125 | Common:2; Rare:73 | ||||
| chr10:30059493-30059697 | Common:1; Rare:74 | ||||
| chr10:30433974-30434221 | Common:2; Rare:62 | ||||
| chr10:30434589-30434702 | Common:1; Rare:33 |