| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:1354779-1355002 | Common:2; Rare:91 | ||||
| chr19:1383437-1383704 | Common:3; Rare:186 | ||||
| chr19:1401477-1401629 | Common:1; Rare:39; Clinvar:1; Clinvar (benign):4 | ||||
| chr19:1438255-1438450 | Rare:78 | ||||
| chr19:1438508-1438891 | Common:1; Rare:150; Clinvar (benign):1 | ||||
| chr19:1449932-1450331 | Common:2; Rare:124 | ||||
| chr19:1479161-1479330 | Common:1; Rare:66 | ||||
| chr19:1479554-1479617 | Rare:14 | ||||
| chr19:1490326-1490489 | Common:3; Rare:58 | ||||
| chr19:1592301-1592456 | Rare:88 | ||||
| chr19:1605397-1605698 | Common:3; Rare:117 | ||||
| chr19:1905135-1905425 | Common:5; Rare:117 | ||||
| chr19:2042024-2042359 | Common:5; Rare:120 | ||||
| chr19:2256385-2256514 | Common:1; Rare:24 | ||||
| chr19:2269232-2269601 | Common:2; Rare:157 |