| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:41940216-41940382 | Common:1; Rare:30 | ||||
| chr22:41998658-41998803 | Common:1; Rare:47 | ||||
| chr22:42070410-42070659 | Common:1; Rare:48; Clinvar:1; Clinvar (benign):1 | ||||
| chr22:42070775-42070971 | Common:2; Rare:41 | ||||
| chr22:42079634-42079865 | Common:1; Rare:83 | ||||
| chr22:42090337-42090532 | Common:1; Rare:42 | ||||
| chr22:42090604-42091054 | Common:2; Rare:180; Clinvar (pathogenic):1 | ||||
| chr22:42432336-42432494 | Rare:37 | ||||
| chr22:42614834-42615253 | Common:3; Rare:184 | ||||
| chr22:42649311-42649482 | Common:1; Rare:67 | ||||
| chr22:42856754-42857043 | Common:2; Rare:84 | ||||
| chr22:42857131-42857430 | Common:3; Rare:116 | ||||
| chr22:42959818-42959969 | Common:1; Rare:29 | ||||
| chr22:42960336-42960405 | Rare:10 | ||||
| chr22:43015079-43015385 | Common:2; Rare:126 |