| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:17638684-17638829 | Rare:51 | ||||
| chr22:18077814-18078076 | Common:5; Rare:85; Clinvar:3; Clinvar (benign):3 | ||||
| chr22:18150054-18150188 | Common:1; Rare:36 | ||||
| chr22:19178250-19178393 | Common:2; Rare:51; Clinvar (benign):4 | ||||
| chr22:19432277-19432563 | Common:3; Rare:115 | ||||
| chr22:19447677-19447926 | Common:2; Rare:103 | ||||
| chr22:19854791-19854983 | Rare:64 | ||||
| chr22:19941779-19941881 | Rare:42; Clinvar:2 | ||||
| chr22:19963140-19963271 | Common:1; Rare:36 | ||||
| chr22:20020899-20021141 | Common:1; Rare:79 | ||||
| chr22:20117175-20117571 | Common:3; Rare:127 | ||||
| chr22:20319972-20320160 | Common:2; Rare:69 | ||||
| chr22:20495781-20495925 | Common:2; Rare:55 | ||||
| chr22:20582939-20583211 | Rare:78 | ||||
| chr22:20858721-20859093 | Common:5; Rare:188; Clinvar:3; Clinvar (benign):3 |