| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:49591591-49591655 | Common:8; Rare:35 | ||||
| chr19:49640199-49640762 | Rare:134 | ||||
| chr19:49641763-49641887 | Rare:24 | ||||
| chr19:49642207-49642320 | Rare:28 | ||||
| chr19:49664423-49664936 | Common:2; Rare:178 | ||||
| chr19:49665567-49665635 | Common:1; Rare:23 | ||||
| chr19:49665703-49666062 | Common:3; Rare:162; Clinvar (pathogenic):1 | ||||
| chr19:49675692-49675892 | Common:1; Rare:30 | ||||
| chr19:49676020-49676198 | Common:1; Rare:35 | ||||
| chr19:49676254-49676451 | Common:3; Rare:39 | ||||
| chr19:49677208-49677363 | Common:1; Rare:67 | ||||
| chr19:49678259-49678535 | Common:1; Rare:44 | ||||
| chr19:49766336-49766517 | Rare:71 | ||||
| chr19:49818051-49818374 | Common:4; Rare:106; Clinvar:3; Clinvar (benign):1 | ||||
| chr19:49850605-49850761 | Rare:39 |