| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:43955285-43955560 | Common:3; Rare:80 | ||||
| chr22:44024127-44024333 | Common:2; Rare:68 | ||||
| chr22:44498172-44498475 | Common:2; Rare:115 | ||||
| chr22:45163654-45164015 | Common:4; Rare:127 | ||||
| chr22:45212371-45212599 | Common:3; Rare:58 | ||||
| chr22:45309663-45309990 | Common:1; Rare:133 | ||||
| chr22:45413554-45413749 | Common:1; Rare:78 | ||||
| chr22:45671954-45672091 | Common:1; Rare:61 | ||||
| chr22:46053727-46053901 | Rare:66 | ||||
| chr22:46054195-46054427 | Common:5; Rare:72 | ||||
| chr22:46250245-46250432 | Common:3; Rare:60 | ||||
| chr22:46267836-46268037 | Common:1; Rare:61 | ||||
| chr22:46296735-46296964 | Common:1; Rare:74 | ||||
| chr22:46335614-46335809 | Common:5; Rare:93; Clinvar:8; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
| chr22:46762447-46762706 | Common:3; Rare:100 |