| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:20116959-20117015 | Common:1; Rare:9 | ||||
| chr22:20117159-20117652 | Common:4; Rare:162 | ||||
| chr22:20319989-20320189 | Common:2; Rare:70 | ||||
| chr22:20495781-20495925 | Common:2; Rare:55 | ||||
| chr22:20858969-20859110 | Common:5; Rare:84; Clinvar:3; Clinvar (benign):5 | ||||
| chr22:20917278-20917484 | Rare:78 | ||||
| chr22:20917647-20917778 | Rare:32 | ||||
| chr22:20982196-20982353 | Common:2; Rare:36; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr22:21002088-21002280 | Common:6; Rare:70 | ||||
| chr22:21629973-21630265 | Common:2; Rare:98 | ||||
| chr22:21642062-21642372 | Common:2; Rare:94 | ||||
| chr22:21938007-21938311 | Rare:98 | ||||
| chr22:23750964-23751159 | Common:1; Rare:72 | ||||
| chr22:23787114-23787214 | Rare:33; Clinvar:2; Clinvar (benign):4 | ||||
| chr22:23857651-23857916 | Common:2; Rare:90 |