| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:42090703-42091129 | Common:4; Rare:299; Clinvar (pathogenic):2 | ||||
| chr22:42519736-42519966 | Common:2; Rare:175 | ||||
| chr22:42553714-42553961 | Common:2; Rare:137 | ||||
| chr22:42614840-42615251 | Common:6; Rare:340 | ||||
| chr22:42648996-42649249 | Rare:64 | ||||
| chr22:42649295-42649594 | Common:6; Rare:103 | ||||
| chr22:42856870-42857090 | Rare:52 | ||||
| chr22:42857176-42857333 | Common:2; Rare:70 | ||||
| chr22:42959804-42959988 | Common:2; Rare:66 | ||||
| chr22:43015057-43015386 | Common:4; Rare:252 | ||||
| chr22:43089327-43089490 | Common:6; Rare:103 | ||||
| chr22:43143313-43143486 | Common:4; Rare:111 | ||||
| chr22:43923506-43923841 | Common:5; Rare:89; Clinvar (benign):3 | ||||
| chr22:43924058-43924614 | Common:2; Rare:141; Clinvar (benign):1 | ||||
| chr22:43955300-43955583 | Common:6; Rare:165 |