| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:20393944-20394196 | Common:1; Rare:78 | ||||
| chr22:20495771-20495973 | Common:2; Rare:73 | ||||
| chr22:20507447-20507630 | Rare:47 | ||||
| chr22:20917275-20917418 | Rare:48 | ||||
| chr22:20917713-20917778 | Rare:13 | ||||
| chr22:20967996-20968185 | Common:3; Rare:69 | ||||
| chr22:20982170-20982353 | Common:2; Rare:50; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr22:21002029-21002271 | Common:5; Rare:94 | ||||
| chr22:21567645-21567758 | Common:1; Rare:44 | ||||
| chr22:21642015-21642372 | Common:2; Rare:109 | ||||
| chr22:21651891-21652232 | Common:2; Rare:72 | ||||
| chr22:21665934-21666070 | Rare:41 | ||||
| chr22:21867643-21867790 | Common:1; Rare:36 | ||||
| chr22:21938093-21938347 | Rare:80 | ||||
| chr22:21952813-21952982 | Common:1; Rare:61 |