| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:20319986-20320133 | Common:2; Rare:56 | ||||
| chr22:20393968-20394217 | Rare:80 | ||||
| chr22:20495754-20495925 | Common:2; Rare:61 | ||||
| chr22:20507490-20507622 | Rare:31 | ||||
| chr22:20982180-20982358 | Common:2; Rare:45; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr22:21002064-21002189 | Common:3; Rare:47 | ||||
| chr22:21651883-21652192 | Common:2; Rare:66 | ||||
| chr22:21665951-21666102 | Common:1; Rare:47 | ||||
| chr22:21867448-21867745 | Common:3; Rare:89 | ||||
| chr22:21937955-21938296 | Rare:103 | ||||
| chr22:21952813-21952969 | Common:1; Rare:58 | ||||
| chr22:21982740-21982887 | Rare:41 | ||||
| chr22:22508717-22508822 | Rare:32 | ||||
| chr22:23145178-23145541 | Common:3; Rare:120 | ||||
| chr22:23786874-23787036 | Common:1; Rare:62; Clinvar:3 |