| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:20917641-20918003 | Common:1; Rare:109 | ||||
| chr22:20982201-20982369 | Common:2; Rare:42; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr22:21002071-21002227 | Common:3; Rare:58 | ||||
| chr22:21867412-21867745 | Common:4; Rare:95 | ||||
| chr22:21938234-21938347 | Rare:37 | ||||
| chr22:23750958-23751206 | Common:2; Rare:84 | ||||
| chr22:23767928-23768062 | Rare:35 | ||||
| chr22:23786875-23787187 | Common:2; Rare:114; Clinvar:6; Clinvar (benign):4 | ||||
| chr22:23787194-23787222 | Rare:5; Clinvar (benign):2 | ||||
| chr22:23857809-23857920 | Common:2; Rare:39 | ||||
| chr22:23894325-23894923 | Common:6; Rare:241; Clinvar:1 | ||||
| chr22:23895119-23895345 | Common:2; Rare:92 | ||||
| chr22:24555877-24556071 | Rare:57 | ||||
| chr22:26477071-26477297 | Rare:56; Clinvar (pathogenic):1 | ||||
| chr22:26483712-26483943 | Common:5; Rare:88; Clinvar:6; Clinvar (benign):2 |