| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:38681816-38682019 | Common:2; Rare:87 | ||||
| chr22:39076976-39077306 | Common:1; Rare:75 | ||||
| chr22:39319596-39319768 | Common:3; Rare:81 | ||||
| chr22:40346441-40346571 | Rare:55; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr22:40636662-40636842 | Rare:54 | ||||
| chr22:40819272-40819544 | Common:11; Rare:122 | ||||
| chr22:40856419-40857162 | Common:3; Rare:304; Clinvar:4 | ||||
| chr22:40951035-40951408 | Common:2; Rare:131 | ||||
| chr22:40951587-40951716 | Common:2; Rare:38 | ||||
| chr22:41286122-41286435 | Common:2; Rare:101 | ||||
| chr22:41446447-41446450 | |||||
| chr22:41446790-41446923 | Rare:49 | ||||
| chr22:41468645-41468798 | Common:2; Rare:43 | ||||
| chr22:41468939-41469167 | Rare:74 | ||||
| chr22:41620982-41621390 | Common:7; Rare:145 |