| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:48170239-48170704 | Common:3; Rare:131 | ||||
| chr19:48445881-48446016 | Rare:48 | ||||
| chr19:48619139-48619428 | Rare:92 | ||||
| chr19:48811005-48811158 | Rare:48 | ||||
| chr19:48872192-48872427 | Common:2; Rare:68 | ||||
| chr19:48993296-48993575 | Common:2; Rare:116; Clinvar:1; Clinvar (benign):1 | ||||
| chr19:49155359-49155551 | Rare:34 | ||||
| chr19:49157666-49157842 | Rare:54; Clinvar:1 | ||||
| chr19:49362379-49362473 | Rare:26 | ||||
| chr19:49453094-49453300 | Common:1; Rare:65 | ||||
| chr19:49580527-49580644 | Rare:43 | ||||
| chr19:49665777-49666034 | Common:2; Rare:131; Clinvar (pathogenic):1 | ||||
| chr19:49808832-49808981 | Rare:50 | ||||
| chr19:49877319-49877717 | Common:1; Rare:99 | ||||
| chr19:49929430-49929567 | Common:4; Rare:50 |