| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:10604653-10604693 | Rare:6 | ||||
| chr19:10653260-10653363 | Common:1; Rare:30 | ||||
| chr19:10864492-10864652 | Rare:40 | ||||
| chr19:10867574-10867696 | Rare:15 | ||||
| chr19:10868040-10868214 | Common:1; Rare:29 | ||||
| chr19:10873020-10873158 | Rare:31 | ||||
| chr19:10876787-10877179 | Rare:84 | ||||
| chr19:10879234-10879352 | Rare:31 | ||||
| chr19:10963635-10963734 | Rare:19 | ||||
| chr19:11179885-11179913 | Rare:5 | ||||
| chr19:11180109-11180301 | Rare:36 | ||||
| chr19:11324405-11324593 | Common:2; Rare:39 | ||||
| chr19:11375507-11375746 | Rare:79 | ||||
| chr19:11377278-11377441 | Rare:42; Clinvar (benign):3 | ||||
| chr19:11424003-11424275 | Rare:76; Clinvar (pathogenic):1 |