| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:19447684-19447977 | Common:2; Rare:113 | ||||
| chr22:19720203-19720453 | Rare:77 | ||||
| chr22:19854826-19854972 | Rare:51 | ||||
| chr22:19941722-19941878 | Rare:66; Clinvar:5; Clinvar (benign):4 | ||||
| chr22:20079921-20080292 | Common:1; Rare:120 | ||||
| chr22:20117334-20117557 | Rare:65 | ||||
| chr22:20319989-20320117 | Common:2; Rare:51 | ||||
| chr22:20495781-20495925 | Common:2; Rare:55 | ||||
| chr22:20507471-20507633 | Rare:45 | ||||
| chr22:20773876-20774143 | Common:2; Rare:43 | ||||
| chr22:20858690-20859066 | Common:5; Rare:179; Clinvar:2; Clinvar (benign):1 | ||||
| chr22:20917132-20917413 | Rare:96 | ||||
| chr22:20982191-20982347 | Common:2; Rare:37; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr22:21002083-21002223 | Common:3; Rare:53 | ||||
| chr22:21665951-21666086 | Rare:41 |