| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:19479125-19479466 | Common:4; Rare:119 | ||||
| chr22:19479693-19479949 | Common:4; Rare:64 | ||||
| chr22:19854795-19854952 | Rare:54 | ||||
| chr22:19941576-19941886 | Common:1; Rare:119; Clinvar:6; Clinvar (benign):7 | ||||
| chr22:20020927-20021151 | Common:1; Rare:73 | ||||
| chr22:20079936-20080299 | Common:1; Rare:122 | ||||
| chr22:20116966-20117557 | Common:4; Rare:170 | ||||
| chr22:20319957-20320137 | Common:2; Rare:72 | ||||
| chr22:20495775-20495994 | Common:2; Rare:82 | ||||
| chr22:20507927-20508069 | Rare:34 | ||||
| chr22:20917278-20917461 | Rare:74 | ||||
| chr22:20982190-20982358 | Common:2; Rare:41; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr22:21002064-21002250 | Common:4; Rare:69 | ||||
| chr22:21642062-21642372 | Common:2; Rare:94 | ||||
| chr22:23750964-23751157 | Common:1; Rare:71 |