| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:49496135-49496496 | Common:1; Rare:129 | ||||
| chr19:49513102-49513271 | Common:1; Rare:37 | ||||
| chr19:49513318-49513412 | Rare:21 | ||||
| chr19:49580524-49580670 | Rare:51 | ||||
| chr19:49665750-49666020 | Common:3; Rare:129; Clinvar (pathogenic):1 | ||||
| chr19:49808808-49808997 | Common:1; Rare:63 | ||||
| chr19:49813245-49813341 | Rare:39 | ||||
| chr19:49850991-49851032 | Rare:17 | ||||
| chr19:49851045-49851120 | Rare:31 | ||||
| chr19:49877251-49877726 | Common:2; Rare:118 | ||||
| chr19:49877839-49878136 | Common:4; Rare:92 | ||||
| chr19:49929423-49929820 | Common:7; Rare:134 | ||||
| chr19:50025325-50025691 | Common:6; Rare:122 | ||||
| chr19:50476234-50476547 | Common:1; Rare:146 | ||||
| chr19:50511137-50511445 | Common:3; Rare:100 |