| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:19479120-19479477 | Common:4; Rare:128 | ||||
| chr22:19854787-19854972 | Rare:63 | ||||
| chr22:19941739-19941886 | Rare:60; Clinvar:4; Clinvar (benign):1 | ||||
| chr22:20020892-20021145 | Common:1; Rare:83 | ||||
| chr22:20117175-20117563 | Common:3; Rare:123 | ||||
| chr22:20319995-20320158 | Common:2; Rare:53 | ||||
| chr22:20495781-20495925 | Common:2; Rare:55 | ||||
| chr22:20734125-20734414 | Rare:76 | ||||
| chr22:20858942-20859113 | Common:5; Rare:95; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr22:20917278-20917461 | Rare:74 | ||||
| chr22:20982191-20982318 | Common:2; Rare:27; Clinvar (benign):2 | ||||
| chr22:21002088-21002240 | Common:3; Rare:56 | ||||
| chr22:21032529-21032663 | Rare:54 | ||||
| chr22:21632585-21632767 | Common:2; Rare:44 | ||||
| chr22:21642062-21642358 | Common:2; Rare:90 |