| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:49676638-49677014 | Common:2; Rare:90 | ||||
| chr19:49677150-49677319 | Common:1; Rare:63 | ||||
| chr19:49677492-49677635 | Rare:44 | ||||
| chr19:49677791-49677805 | Rare:3 | ||||
| chr19:49690940-49691132 | Rare:45 | ||||
| chr19:49766226-49766534 | Rare:98 | ||||
| chr19:49766857-49767103 | Common:1; Rare:87 | ||||
| chr19:49808816-49809075 | Common:2; Rare:71 | ||||
| chr19:49809233-49809392 | Rare:41 | ||||
| chr19:49809488-49809542 | Rare:13 | ||||
| chr19:49817426-49817632 | Common:2; Rare:50 | ||||
| chr19:49818250-49818384 | Common:3; Rare:69; Clinvar:3; Clinvar (benign):1 | ||||
| chr19:49850572-49850823 | Rare:67 | ||||
| chr19:49850895-49851307 | Common:2; Rare:162 | ||||
| chr19:49851440-49851787 | Common:1; Rare:109 |