| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:37779565-37779675 | Rare:25 | ||||
| chr19:37817275-37817473 | Common:1; Rare:38 | ||||
| chr19:37907051-37907293 | Rare:53 | ||||
| chr19:38228199-38228415 | Common:3; Rare:39 | ||||
| chr19:38315907-38316104 | Rare:59 | ||||
| chr19:38336332-38336454 | Common:1; Rare:25 | ||||
| chr19:38336882-38337156 | Common:3; Rare:57 | ||||
| chr19:38374406-38374817 | Rare:155 | ||||
| chr19:38618834-38619316 | Common:4; Rare:135 | ||||
| chr19:38631845-38632019 | Common:1; Rare:50 | ||||
| chr19:38647372-38647740 | Common:3; Rare:130 | ||||
| chr19:38831765-38832074 | Common:4; Rare:90; Clinvar (benign):1 | ||||
| chr19:38849264-38849495 | Rare:92 | ||||
| chr19:38852314-38852468 | Rare:45 | ||||
| chr19:38899517-38900018 | Rare:153 |