| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:20394013-20394217 | Rare:108 | ||||
| chr22:20437781-20438020 | Rare:84 | ||||
| chr22:20495745-20496012 | Common:5; Rare:176 | ||||
| chr22:20507455-20507701 | Rare:166 | ||||
| chr22:20566540-20567020 | Rare:222 | ||||
| chr22:20773979-20774137 | Rare:29 | ||||
| chr22:20858260-20858670 | Common:4; Rare:190 | ||||
| chr22:20858715-20859126 | Common:13; Rare:406; Clinvar:7; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
| chr22:20917279-20917524 | Rare:168 | ||||
| chr22:20917796-20918360 | Common:1; Rare:272 | ||||
| chr22:20964881-20965203 | Common:4; Rare:137 | ||||
| chr22:20981918-20982034 | Rare:73 | ||||
| chr22:20982191-20982408 | Common:4; Rare:109; Clinvar:1; Clinvar (benign):8; Clinvar (pathogenic):3 | ||||
| chr22:21002002-21002303 | Common:10; Rare:198 | ||||
| chr22:21014190-21014630 | Rare:114 |