| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:35257747-35257942 | Rare:58 | ||||
| chr22:35299687-35299964 | Common:2; Rare:72 | ||||
| chr22:35300108-35300363 | Common:2; Rare:73 | ||||
| chr22:35380963-35381242 | Common:1; Rare:84 | ||||
| chr22:35399873-35400229 | Rare:126 | ||||
| chr22:35410132-35410395 | Common:2; Rare:60 | ||||
| chr22:35647925-35648133 | Common:1; Rare:40 | ||||
| chr22:35648264-35648567 | Common:2; Rare:53 | ||||
| chr22:35648585-35648753 | Common:1; Rare:37 | ||||
| chr22:35648881-35649022 | Rare:18 | ||||
| chr22:36160567-36160917 | Common:5; Rare:123 | ||||
| chr22:36239440-36239869 | Common:3; Rare:117 | ||||
| chr22:36252973-36253177 | Rare:42 | ||||
| chr22:36387848-36388474 | Common:6; Rare:172; Clinvar:2; Clinvar (benign):1 | ||||
| chr22:36481263-36481463 | Common:2; Rare:42 |