| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:43635750-43635887 | Common:1; Rare:33 | ||||
| chr6:43687757-43687860 | Common:1; Rare:42 | ||||
| chr6:43770081-43770230 | Common:2; Rare:45 | ||||
| chr6:43771901-43772022 | Rare:21 | ||||
| chr6:44127369-44127644 | Common:4; Rare:78 | ||||
| chr6:44223442-44223615 | Common:1; Rare:51 | ||||
| chr6:44246880-44247192 | Common:4; Rare:131 | ||||
| chr6:44387445-44387753 | Common:4; Rare:82 | ||||
| chr6:46129784-46130103 | Common:5; Rare:102 | ||||
| chr6:46652737-46653013 | Rare:72 | ||||
| chr6:47309934-47310089 | Common:1; Rare:38 | ||||
| chr6:47477476-47477793 | Rare:93 | ||||
| chr6:47478067-47478255 | Common:2; Rare:67; Clinvar:2; Clinvar (benign):3 | ||||
| chr6:49463148-49463431 | Common:1; Rare:80; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:52284667-52285019 | Common:2; Rare:122 |