| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:19447677-19447761 | Common:1; Rare:44 | ||||
| chr22:19479142-19479466 | Common:4; Rare:111 | ||||
| chr22:19719090-19719147 | Rare:21 | ||||
| chr22:19854787-19854972 | Rare:63 | ||||
| chr22:19941710-19941878 | Rare:73; Clinvar:6; Clinvar (benign):4 | ||||
| chr22:20117175-20117571 | Common:3; Rare:127 | ||||
| chr22:20319994-20320104 | Common:2; Rare:42 | ||||
| chr22:20495781-20495984 | Common:2; Rare:78 | ||||
| chr22:20507516-20507622 | Rare:25 | ||||
| chr22:20858684-20859113 | Common:8; Rare:212; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr22:20982183-20982363 | Common:2; Rare:46; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr22:21002088-21002219 | Common:3; Rare:49 | ||||
| chr22:21629982-21630353 | Common:4; Rare:111 | ||||
| chr22:21642070-21642366 | Common:2; Rare:90 | ||||
| chr22:21938203-21938345 | Rare:43 |