| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:39824380-39824813 | Common:4; Rare:131 | ||||
| chr19:39881648-39881756 | Common:3; Rare:18 | ||||
| chr19:39936035-39936256 | Rare:38 | ||||
| chr19:39937119-39937267 | Rare:26 | ||||
| chr19:39941571-39941794 | Common:1; Rare:43 | ||||
| chr19:39941873-39942123 | Common:1; Rare:31 | ||||
| chr19:39944069-39944401 | Common:2; Rare:52 | ||||
| chr19:39996453-39996523 | Common:1; Rare:16 | ||||
| chr19:40143687-40143804 | Common:1; Rare:26 | ||||
| chr19:40144277-40144467 | Rare:32 | ||||
| chr19:40147656-40147847 | Common:1; Rare:35 | ||||
| chr19:40190600-40190838 | Common:1; Rare:36 | ||||
| chr19:40190898-40191135 | Rare:52 | ||||
| chr19:40356104-40356322 | Rare:38 | ||||
| chr19:40403544-40403784 | Common:2; Rare:82; Clinvar:3; Clinvar (benign):2 |