| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:35330244-35330476 | Common:1; Rare:66 | ||||
| chr22:35382996-35383231 | Common:1; Rare:63 | ||||
| chr22:36288725-36289301 | Common:2; Rare:174; Clinvar:6; Clinvar (benign):10 | ||||
| chr22:36305969-36306329 | Common:3; Rare:92; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr22:36323202-36323538 | Common:3; Rare:60 | ||||
| chr22:36324783-36324796 | |||||
| chr22:36330680-36330860 | Common:1; Rare:37 | ||||
| chr22:36385979-36386111 | Rare:25 | ||||
| chr22:37624862-37625076 | Rare:50 | ||||
| chr22:38740999-38741236 | Rare:50 | ||||
| chr22:38741492-38741627 | Common:1; Rare:37; Clinvar (benign):1 | ||||
| chr22:41170288-41170569 | Rare:63; Clinvar:1; Clinvar (benign):1 | ||||
| chr22:41172231-41172604 | Common:3; Rare:80; Clinvar (benign):2 | ||||
| chr22:41197429-41197621 | Common:1; Rare:46 | ||||
| chr22:41256020-41256246 | Rare:73 |