| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:21735712-21736195 | Common:3; Rare:171 | ||||
| chr22:21867609-21867917 | Common:2; Rare:99 | ||||
| chr22:21938078-21938271 | Rare:64 | ||||
| chr22:21952802-21952985 | Common:1; Rare:67 | ||||
| chr22:21982731-21982918 | Rare:51 | ||||
| chr22:22508702-22508914 | Rare:69 | ||||
| chr22:23070050-23070390 | Common:1; Rare:131 | ||||
| chr22:23070567-23071129 | Common:2; Rare:153 | ||||
| chr22:23141962-23142280 | Common:5; Rare:77 | ||||
| chr22:23145120-23145530 | Common:3; Rare:138 | ||||
| chr22:23751073-23751296 | Common:3; Rare:70 | ||||
| chr22:23767936-23768073 | Rare:35 | ||||
| chr22:23772727-23772873 | Rare:47 | ||||
| chr22:23786843-23787027 | Common:2; Rare:65; Clinvar:3 | ||||
| chr22:23787241-23787461 | Common:7; Rare:102; Clinvar:1; Clinvar (benign):3 |