| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:38739837-38740196 | Rare:83; Clinvar (benign):1 | ||||
| chr22:38952572-38952743 | Rare:29 | ||||
| chr22:39014148-39014310 | Rare:42 | ||||
| chr22:39244958-39245133 | Rare:42 | ||||
| chr22:39502077-39502379 | Rare:82 | ||||
| chr22:40044121-40044327 | Common:2; Rare:44 | ||||
| chr22:40346409-40346580 | Common:1; Rare:77; Clinvar:5; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr22:40636668-40636996 | Common:2; Rare:95 | ||||
| chr22:40856721-40857154 | Common:2; Rare:160; Clinvar:3 | ||||
| chr22:41091413-41091758 | Common:5; Rare:121 | ||||
| chr22:41286175-41286424 | Common:2; Rare:74 | ||||
| chr22:41468965-41469159 | Rare:61 | ||||
| chr22:41621057-41621379 | Common:6; Rare:115 | ||||
| chr22:41800496-41800631 | Rare:46 | ||||
| chr22:41832909-41833273 | Common:3; Rare:131 |