| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:45240825-45241196 | Common:6; Rare:115 | ||||
| chr22:45309658-45310031 | Common:2; Rare:274 | ||||
| chr22:45413589-45413747 | Common:1; Rare:62 | ||||
| chr22:45502503-45502975 | Common:4; Rare:249 | ||||
| chr22:45671755-45671914 | Common:2; Rare:51 | ||||
| chr22:45672130-45673250 | Common:18; Rare:487 | ||||
| chr22:45688576-45689050 | Common:5; Rare:154 | ||||
| chr22:46053701-46053919 | Rare:116 | ||||
| chr22:46150250-46150632 | Common:2; Rare:217 | ||||
| chr22:46250201-46250487 | Common:6; Rare:148 | ||||
| chr22:46267805-46268038 | Common:2; Rare:129 | ||||
| chr22:46296626-46297009 | Common:6; Rare:229 | ||||
| chr22:46335590-46335970 | Common:16; Rare:326; Clinvar:24; Clinvar (benign):20; Clinvar (pathogenic):4 | ||||
| chr22:46537397-46537956 | Common:7; Rare:256 | ||||
| chr22:46575976-46576181 | Common:4; Rare:53 |