| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:18024501-18024646 | Rare:46 | ||||
| chr22:18077814-18078032 | Common:4; Rare:73; Clinvar:3; Clinvar (benign):2 | ||||
| chr22:18149835-18150125 | Common:2; Rare:69 | ||||
| chr22:19291696-19291921 | Common:10; Rare:69 | ||||
| chr22:19432303-19432603 | Common:4; Rare:129 | ||||
| chr22:19854795-19854997 | Rare:71 | ||||
| chr22:19941722-19941886 | Rare:69; Clinvar:5; Clinvar (benign):4 | ||||
| chr22:20079916-20080292 | Common:1; Rare:120 | ||||
| chr22:20116972-20117621 | Common:3; Rare:193 | ||||
| chr22:20319986-20320158 | Common:2; Rare:60 | ||||
| chr22:20394060-20394196 | Rare:33 | ||||
| chr22:20495775-20495935 | Common:2; Rare:61 | ||||
| chr22:20507490-20507681 | Rare:72 | ||||
| chr22:20582852-20583159 | Rare:90 | ||||
| chr22:20858696-20859184 | Common:9; Rare:241; Clinvar:4; Clinvar (benign):6; Clinvar (pathogenic):1 |