| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:17643871-17644276 | Common:2; Rare:122 | ||||
| chr10:18651582-18651715 | Common:1; Rare:54 | ||||
| chr10:22325554-22325671 | Rare:55 | ||||
| chr10:26438216-26438357 | Common:1; Rare:30 | ||||
| chr10:27100432-27100617 | Common:3; Rare:53; Clinvar:4; Clinvar (benign):2 | ||||
| chr10:27154314-27154436 | Rare:32 | ||||
| chr10:27155227-27155391 | Common:3; Rare:58; Clinvar:2; Clinvar (benign):3 | ||||
| chr10:27242083-27242221 | Common:1; Rare:56 | ||||
| chr10:28532474-28532862 | Common:5; Rare:156 | ||||
| chr10:30059529-30059671 | Rare:58 | ||||
| chr10:31318999-31319260 | Common:2; Rare:73 | ||||
| chr10:31928724-31928950 | Common:3; Rare:91 | ||||
| chr10:32958144-32958432 | Common:2; Rare:111 | ||||
| chr10:35126722-35127165 | Common:4; Rare:144 | ||||
| chr10:37976519-37976798 | Common:2; Rare:74 |