| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:50804572-50804913 | Common:8; Rare:106 | ||||
| chr19:51108372-51108623 | Common:1; Rare:57 | ||||
| chr19:51124783-51124971 | Rare:50 | ||||
| chr19:51124983-51125225 | Rare:84 | ||||
| chr19:51142286-51142370 | Rare:27 | ||||
| chr19:51142398-51142630 | Rare:64 | ||||
| chr19:51224865-51225181 | Common:3; Rare:78 | ||||
| chr19:51366323-51366562 | Common:5; Rare:69; Clinvar (benign):2 | ||||
| chr19:51367570-51367884 | Common:1; Rare:93 | ||||
| chr19:51372593-51372826 | Common:2; Rare:32 | ||||
| chr19:51501684-51501880 | Rare:58 | ||||
| chr19:51646027-51646212 | Common:1; Rare:26 | ||||
| chr19:51751818-51752114 | Common:2; Rare:66 | ||||
| chr19:51752244-51752504 | Common:1; Rare:52 | ||||
| chr19:51927413-51927534 | Common:1; Rare:32 |