| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:43179621-43179940 | Common:4; Rare:135 | ||||
| chr22:45827288-45827357 | Common:1; Rare:9 | ||||
| chr22:45827404-45827687 | Common:1; Rare:49 | ||||
| chr22:46056596-46056803 | Rare:24 | ||||
| chr22:46080061-46080403 | Common:1; Rare:106 | ||||
| chr22:46082200-46082342 | Common:3; Rare:26 | ||||
| chr22:47631598-47631747 | Common:2; Rare:43 | ||||
| chr22:50216676-50217320 | Common:7; Rare:369 | ||||
| chr3:4831350-4831483 | Common:1; Rare:20 | ||||
| chr3:9381651-9381941 | Common:6; Rare:47 | ||||
| chr3:9453818-9454048 | Rare:41; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:9460089-9460388 | Common:2; Rare:61 | ||||
| chr3:9466310-9466424 | Common:1; Rare:16 | ||||
| chr3:9762994-9763294 | Common:1; Rare:92 | ||||
| chr3:9784086-9784356 | Rare:74 |