| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:34676940-34677093 | Rare:18 | ||||
| chr19:35003345-35003518 | Rare:46 | ||||
| chr19:35086032-35086254 | Rare:43 | ||||
| chr19:35124568-35124722 | Common:2; Rare:41 | ||||
| chr19:35155723-35155819 | Common:1; Rare:28 | ||||
| chr19:35205379-35205591 | Common:1; Rare:46 | ||||
| chr19:35206452-35206732 | Common:1; Rare:53 | ||||
| chr19:35267657-35267769 | Rare:53 | ||||
| chr19:35267990-35268194 | Common:6; Rare:84 | ||||
| chr19:35272479-35272584 | Rare:20 | ||||
| chr19:35295856-35295999 | Common:2; Rare:56; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr19:35330519-35330879 | Common:1; Rare:73 | ||||
| chr19:35334203-35334489 | Common:6; Rare:41 | ||||
| chr19:35335040-35335149 | Common:1; Rare:13 | ||||
| chr19:35347537-35347921 | Common:1; Rare:73 |