| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:1275735-1276176 | Common:6; Rare:499 | ||||
| chr19:1354684-1355061 | Common:10; Rare:424 | ||||
| chr19:1373383-1373783 | Common:7; Rare:192 | ||||
| chr19:1383411-1384201 | Common:7; Rare:672; Clinvar (benign):4 | ||||
| chr19:1407127-1407991 | Common:6; Rare:573 | ||||
| chr19:1415390-1415900 | Common:5; Rare:163 | ||||
| chr19:1438243-1438522 | Common:1; Rare:121 | ||||
| chr19:1445951-1446275 | Common:3; Rare:140 | ||||
| chr19:1479108-1479382 | Common:2; Rare:220 | ||||
| chr19:1479470-1479710 | Common:2; Rare:113 | ||||
| chr19:1490254-1490531 | Common:7; Rare:172 | ||||
| chr19:1507794-1508012 | Rare:140 | ||||
| chr19:1508064-1508491 | Common:7; Rare:143 | ||||
| chr19:1512958-1513196 | Common:4; Rare:186 | ||||
| chr19:1513210-1513580 | Common:4; Rare:154 |