| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:38505992-38506082 | Common:1; Rare:39 | ||||
| chr22:38570171-38570483 | Common:5; Rare:57 | ||||
| chr22:38656401-38656706 | Common:1; Rare:66 | ||||
| chr22:38681851-38682017 | Common:1; Rare:74 | ||||
| chr22:39502138-39502397 | Rare:72 | ||||
| chr22:40044548-40044892 | Common:2; Rare:77 | ||||
| chr22:40346458-40346649 | Rare:91; Clinvar:9; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr22:40636644-40637012 | Common:2; Rare:102 | ||||
| chr22:40819321-40819559 | Common:11; Rare:113 | ||||
| chr22:40856768-40857154 | Common:2; Rare:146; Clinvar:3 | ||||
| chr22:40951029-40951401 | Common:2; Rare:130 | ||||
| chr22:41091708-41091841 | Common:1; Rare:56 | ||||
| chr22:41286158-41286447 | Common:2; Rare:89 | ||||
| chr22:41301207-41301610 | Common:2; Rare:108 | ||||
| chr22:41367158-41367483 | Rare:92 |