| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:38681783-38682026 | Common:2; Rare:101 | ||||
| chr22:38982170-38982421 | Common:2; Rare:50 | ||||
| chr22:39244969-39245195 | Rare:48 | ||||
| chr22:39319594-39319768 | Common:3; Rare:81 | ||||
| chr22:39349820-39350017 | Common:1; Rare:59 | ||||
| chr22:39502140-39502412 | Rare:80 | ||||
| chr22:40044129-40044362 | Common:2; Rare:54 | ||||
| chr22:40346445-40346556 | Rare:47; Clinvar:2; Clinvar (benign):2 | ||||
| chr22:40636696-40637031 | Common:2; Rare:89 | ||||
| chr22:40856721-40857164 | Common:3; Rare:166; Clinvar:4 | ||||
| chr22:40951156-40951413 | Common:1; Rare:83 | ||||
| chr22:40951574-40951716 | Common:2; Rare:46 | ||||
| chr22:41091413-41091825 | Common:6; Rare:145 | ||||
| chr22:41286142-41286432 | Common:2; Rare:93 | ||||
| chr22:41367181-41367459 | Rare:82 |