| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:36973453-36973605 | Common:2; Rare:31 | ||||
| chr19:37078173-37078465 | Common:2; Rare:69 | ||||
| chr19:37317653-37317920 | Common:6; Rare:64 | ||||
| chr19:37467190-37467537 | Common:2; Rare:99 | ||||
| chr19:37469270-37469421 | Common:2; Rare:39 | ||||
| chr19:37594734-37594882 | Rare:41 | ||||
| chr19:37779584-37779675 | Rare:18 | ||||
| chr19:38319843-38319884 | Rare:10 | ||||
| chr19:38647370-38647756 | Common:3; Rare:132 | ||||
| chr19:38723993-38724333 | Rare:118; Clinvar:1; Clinvar (benign):3 | ||||
| chr19:38842209-38842462 | Rare:49 | ||||
| chr19:38849882-38849923 | Common:2; Rare:28 | ||||
| chr19:38852314-38852582 | Rare:69 | ||||
| chr19:38899531-38900077 | Rare:165 | ||||
| chr19:38930715-38931002 | Common:3; Rare:85; Clinvar:2; Clinvar (benign):3 |