| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:49149377-49149576 | Common:1; Rare:70 | ||||
| chr19:49157689-49157850 | Rare:47; Clinvar:1 | ||||
| chr19:49335318-49335406 | Rare:14 | ||||
| chr19:49362363-49362473 | Rare:30 | ||||
| chr19:49388081-49388269 | Common:3; Rare:75 | ||||
| chr19:49453094-49453302 | Common:1; Rare:66 | ||||
| chr19:49453481-49453588 | Rare:30 | ||||
| chr19:49512537-49512726 | Rare:43 | ||||
| chr19:49513102-49513403 | Common:1; Rare:69 | ||||
| chr19:49527864-49528024 | Common:3; Rare:47 | ||||
| chr19:49580534-49580620 | Rare:28 | ||||
| chr19:49581318-49581351 | Common:1; Rare:6 | ||||
| chr19:49665777-49666041 | Common:2; Rare:133; Clinvar (pathogenic):1 | ||||
| chr19:49808786-49808997 | Common:2; Rare:69 | ||||
| chr19:49813249-49813341 | Rare:38 |