| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:49580515-49580650 | Rare:49 | ||||
| chr19:49665759-49666034 | Common:3; Rare:133; Clinvar (pathogenic):1 | ||||
| chr19:49813258-49813328 | Rare:31 | ||||
| chr19:49851068-49851120 | Rare:21 | ||||
| chr19:49857534-49857775 | Common:3; Rare:93 | ||||
| chr19:49867255-49867415 | Common:2; Rare:39 | ||||
| chr19:49877247-49877743 | Common:2; Rare:129 | ||||
| chr19:49877910-49878168 | Common:2; Rare:84 | ||||
| chr19:49929111-49929205 | Common:3; Rare:32 | ||||
| chr19:49929423-49929567 | Common:4; Rare:52 | ||||
| chr19:50476216-50476547 | Common:1; Rare:156 | ||||
| chr19:50804587-50804909 | Common:6; Rare:97 | ||||
| chr19:51125000-51125149 | Rare:55 | ||||
| chr19:51225001-51225139 | Rare:34 | ||||
| chr19:51366276-51366551 | Common:5; Rare:83; Clinvar (benign):2 |