| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:663147-663455 | Common:2; Rare:126 | ||||
| chr19:708769-709149 | Common:3; Rare:110 | ||||
| chr19:821913-822137 | Rare:63 | ||||
| chr19:893167-893484 | Common:3; Rare:132 | ||||
| chr19:984207-984386 | Common:3; Rare:68 | ||||
| chr19:1103802-1104104 | Common:4; Rare:127 | ||||
| chr19:1260955-1261173 | Common:3; Rare:71 | ||||
| chr19:1266612-1266697 | Common:1; Rare:30 | ||||
| chr19:1269057-1269407 | Common:2; Rare:134 | ||||
| chr19:1354786-1355017 | Common:3; Rare:106 | ||||
| chr19:1383437-1383523 | Common:1; Rare:40 | ||||
| chr19:1401496-1401623 | Common:1; Rare:34; Clinvar:1; Clinvar (benign):4 | ||||
| chr19:1451953-1452190 | Rare:62 | ||||
| chr19:1453105-1453266 | Common:3; Rare:52 | ||||
| chr19:1490321-1490507 | Common:3; Rare:66 |