| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:4575752-4576090 | Rare:100; Clinvar:1 | ||||
| chr9:4576845-4577088 | Common:2; Rare:53 | ||||
| chr9:4578161-4578250 | Common:1; Rare:16 | ||||
| chr9:4580067-4580156 | Rare:18 | ||||
| chr9:4582870-4583166 | Common:1; Rare:91; Clinvar:5; Clinvar (pathogenic):1 | ||||
| chr9:4584995-4585393 | Rare:113; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr9:5768852-5769015 | Rare:56 | ||||
| chr9:5780624-5780840 | Common:2; Rare:59 | ||||
| chr9:14297060-14297236 | Rare:38 | ||||
| chr9:15478539-15478564 | Rare:7 | ||||
| chr9:15479625-15479873 | Common:1; Rare:77 | ||||
| chr9:21559769-21559934 | Rare:93 | ||||
| chr9:22008680-22008739 | Rare:31 | ||||
| chr9:22113379-22113619 | Common:1; Rare:52 | ||||
| chr9:22117687-22117911 | Rare:40 |