| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:42857184-42857424 | Common:3; Rare:97 | ||||
| chr22:43089325-43089496 | Common:3; Rare:55 | ||||
| chr22:43151479-43151585 | Rare:24 | ||||
| chr22:43812208-43812441 | Common:3; Rare:78 | ||||
| chr22:43862389-43862660 | Common:8; Rare:115 | ||||
| chr22:43955300-43955562 | Common:3; Rare:79 | ||||
| chr22:44024165-44024335 | Common:1; Rare:60 | ||||
| chr22:44498166-44498475 | Common:2; Rare:117 | ||||
| chr22:45163700-45164003 | Common:4; Rare:111 | ||||
| chr22:45309716-45309955 | Common:1; Rare:94 | ||||
| chr22:45413605-45413753 | Common:1; Rare:54 | ||||
| chr22:46053668-46053878 | Rare:70 | ||||
| chr22:46267865-46268053 | Common:1; Rare:63 | ||||
| chr22:46296745-46296918 | Rare:57 | ||||
| chr22:46335621-46335792 | Common:4; Rare:78; Clinvar:5; Clinvar (benign):8; Clinvar (pathogenic):1 |