| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:42070802-42070948 | Common:2; Rare:31 | ||||
| chr22:42079505-42079771 | Common:2; Rare:72 | ||||
| chr22:42090685-42090967 | Common:2; Rare:123; Clinvar (pathogenic):1 | ||||
| chr22:42553695-42553923 | Common:1; Rare:67 | ||||
| chr22:42614857-42615246 | Common:3; Rare:161 | ||||
| chr22:42649333-42649482 | Common:1; Rare:58 | ||||
| chr22:42857178-42857430 | Common:3; Rare:105 | ||||
| chr22:43089314-43089496 | Common:3; Rare:62 | ||||
| chr22:43151471-43151590 | Common:1; Rare:29 | ||||
| chr22:43812269-43812441 | Common:2; Rare:58 | ||||
| chr22:43862389-43862651 | Common:8; Rare:110 | ||||
| chr22:43955297-43955556 | Common:3; Rare:76 | ||||
| chr22:44498080-44498469 | Common:3; Rare:138 | ||||
| chr22:45163758-45164003 | Common:2; Rare:95 | ||||
| chr22:46053597-46053863 | Rare:87 |