| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:20507763-20508210 | Common:1; Rare:219 | ||||
| chr22:20523138-20523865 | Common:13; Rare:203 | ||||
| chr22:20566290-20566970 | Common:2; Rare:180 | ||||
| chr22:20858250-20858670 | Common:10; Rare:355 | ||||
| chr22:20858667-20859165 | Common:42; Rare:1209; Clinvar:20; Clinvar (benign):25; Clinvar (pathogenic):3 | ||||
| chr22:20859319-20859574 | Rare:72; Clinvar (benign):1 | ||||
| chr22:20916740-20917227 | Common:1; Rare:227 | ||||
| chr22:20917165-20917560 | Rare:643 | ||||
| chr22:20917501-20918152 | Common:1; Rare:405 | ||||
| chr22:20981468-20982076 | Common:11; Rare:425; Clinvar (benign):1 | ||||
| chr22:20982080-20982435 | Common:14; Rare:457; Clinvar:3; Clinvar (benign):24; Clinvar (pathogenic):9 | ||||
| chr22:20982410-20982690 | Common:1; Rare:121; Clinvar:3; Clinvar (pathogenic):4 | ||||
| chr22:21000922-21001322 | Common:1; Rare:124 | ||||
| chr22:21001578-21002816 | Common:72; Rare:1904 | ||||
| chr22:21014246-21015576 | Common:6; Rare:601 |