| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:20117159-20117630 | Common:3; Rare:155 | ||||
| chr22:20319992-20320158 | Common:2; Rare:55 | ||||
| chr22:20495787-20495920 | Common:1; Rare:50 | ||||
| chr22:20858702-20859110 | Common:8; Rare:207; Clinvar:3; Clinvar (benign):5 | ||||
| chr22:20917287-20917484 | Rare:73 | ||||
| chr22:20982201-20982358 | Common:2; Rare:35; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr22:21002101-21002256 | Common:4; Rare:55 | ||||
| chr22:21938323-21938370 | Rare:6 | ||||
| chr22:21952791-21953126 | Common:2; Rare:103 | ||||
| chr22:23145450-23145539 | Common:1; Rare:40 | ||||
| chr22:23283943-23284015 | Common:1; Rare:17 | ||||
| chr22:23767940-23768051 | Rare:30 | ||||
| chr22:23857671-23857920 | Common:2; Rare:90 | ||||
| chr22:23894200-23894492 | Common:4; Rare:102 | ||||
| chr22:23894565-23894907 | Common:3; Rare:141; Clinvar:1 |