| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:19963194-19963291 | Common:1; Rare:21 | ||||
| chr22:20020873-20021173 | Common:1; Rare:99 | ||||
| chr22:20079914-20080299 | Common:1; Rare:126 | ||||
| chr22:20116951-20117012 | Common:1; Rare:14 | ||||
| chr22:20117146-20117571 | Common:3; Rare:136 | ||||
| chr22:20319994-20320159 | Common:2; Rare:54 | ||||
| chr22:20495781-20495994 | Common:2; Rare:81 | ||||
| chr22:20507458-20507647 | Rare:59 | ||||
| chr22:20858736-20859121 | Common:7; Rare:193; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr22:20917278-20917490 | Rare:78 | ||||
| chr22:20982170-20982358 | Common:2; Rare:51; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr22:21002088-21002215 | Common:3; Rare:49 | ||||
| chr22:21630041-21630335 | Common:3; Rare:75 | ||||
| chr22:21642034-21642408 | Common:2; Rare:118 | ||||
| chr22:23283502-23283802 | Common:2; Rare:53 |