| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:20582684-20583152 | Rare:152 | ||||
| chr22:20858721-20859121 | Common:7; Rare:201; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr22:20917278-20917484 | Rare:78 | ||||
| chr22:20982190-20982353 | Common:2; Rare:40; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr22:21002029-21002259 | Common:4; Rare:90 | ||||
| chr22:21629989-21630056 | Common:1; Rare:38 | ||||
| chr22:21642042-21642372 | Common:2; Rare:102 | ||||
| chr22:21867176-21867289 | Common:1; Rare:35 | ||||
| chr22:21938025-21938345 | Rare:96 | ||||
| chr22:21940678-21940962 | Common:1; Rare:48 | ||||
| chr22:22887680-22888011 | Common:7; Rare:109 | ||||
| chr22:23145192-23145524 | Common:3; Rare:114 | ||||
| chr22:23750972-23751227 | Common:2; Rare:88 | ||||
| chr22:23767940-23768032 | Rare:27 | ||||
| chr22:23838944-23839068 | Rare:56 |