| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:42649077-42649683 | Common:9; Rare:176 | ||||
| chr22:42720639-42721051 | Common:5; Rare:113 | ||||
| chr22:42856667-42857083 | Common:2; Rare:110 | ||||
| chr22:42857134-42857484 | Common:3; Rare:137 | ||||
| chr22:43015052-43015460 | Common:2; Rare:164 | ||||
| chr22:43089276-43089544 | Common:4; Rare:87 | ||||
| chr22:43110603-43110802 | Common:3; Rare:58 | ||||
| chr22:43111235-43111435 | Common:1; Rare:46 | ||||
| chr22:43143292-43143566 | Common:5; Rare:77 | ||||
| chr22:43151438-43151623 | Common:2; Rare:40 | ||||
| chr22:43186548-43186687 | Common:1; Rare:37 | ||||
| chr22:43187564-43187859 | Common:5; Rare:94 | ||||
| chr22:43812220-43812567 | Common:4; Rare:114 | ||||
| chr22:43923553-43923816 | Common:4; Rare:74; Clinvar (benign):3 | ||||
| chr22:43955198-43955601 | Common:5; Rare:120 |