| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:38872176-38872296 | Rare:30 | ||||
| chr22:39020806-39020923 | Common:1; Rare:33 | ||||
| chr22:39021403-39021483 | Rare:28 | ||||
| chr22:39319594-39319808 | Common:3; Rare:94 | ||||
| chr22:39502138-39502379 | Rare:66 | ||||
| chr22:39521048-39521199 | Common:2; Rare:51 | ||||
| chr22:39532661-39532898 | Common:2; Rare:103 | ||||
| chr22:40044160-40044341 | Common:2; Rare:37 | ||||
| chr22:40044528-40044874 | Common:2; Rare:81 | ||||
| chr22:40346441-40346655 | Rare:98; Clinvar:9; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr22:40636651-40637022 | Common:2; Rare:102 | ||||
| chr22:40819283-40819523 | Common:11; Rare:112 | ||||
| chr22:40856434-40857154 | Common:2; Rare:291; Clinvar:3 | ||||
| chr22:41091456-41091882 | Common:7; Rare:154 | ||||
| chr22:41286164-41286424 | Common:2; Rare:79 |