| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:27793667-27794025 | Rare:93 | ||||
| chr19:35730495-35730787 | Common:1; Rare:69; Clinvar (pathogenic):1 | ||||
| chr19:36142710-36142952 | Rare:57 | ||||
| chr19:36797291-36797542 | Rare:54 | ||||
| chr19:38251163-38251293 | Rare:32 | ||||
| chr19:38251424-38251482 | Rare:13 | ||||
| chr19:39409641-39409829 | Common:1; Rare:43 | ||||
| chr19:41352929-41352982 | Common:1; Rare:18; Clinvar (benign):1 | ||||
| chr19:41500618-41500739 | Rare:19 | ||||
| chr19:42396905-42397176 | Common:1; Rare:63 | ||||
| chr19:45509338-45509377 | Rare:16 | ||||
| chr19:46404231-46404358 | Common:1; Rare:28 | ||||
| chr19:46428870-46429052 | Common:1; Rare:33 | ||||
| chr19:46860822-46861127 | Common:3; Rare:99 | ||||
| chr19:47270468-47270651 | Common:3; Rare:67 |