| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:15860479-15860589 | Rare:28 | ||||
| chr10:17230602-17230710 | Rare:40; Clinvar:1 | ||||
| chr10:17643898-17644276 | Common:2; Rare:112 | ||||
| chr10:18140478-18140801 | Common:2; Rare:103; Clinvar:3; Clinvar (benign):5 | ||||
| chr10:27100469-27100587 | Common:2; Rare:37; Clinvar:1; Clinvar (benign):1 | ||||
| chr10:27154221-27154489 | Rare:73 | ||||
| chr10:27155227-27155391 | Common:3; Rare:58; Clinvar:2; Clinvar (benign):3 | ||||
| chr10:27240478-27240560 | Rare:34 | ||||
| chr10:27240565-27240653 | Common:2; Rare:22 | ||||
| chr10:27242058-27242211 | Common:1; Rare:66 | ||||
| chr10:28532466-28533175 | Common:6; Rare:267 | ||||
| chr10:28533411-28533517 | Rare:30 | ||||
| chr10:28677274-28677531 | Common:6; Rare:121 | ||||
| chr10:30059514-30059618 | Common:1; Rare:44 | ||||
| chr10:31031841-31032028 | Common:1; Rare:72 |