| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:18940285-18940504 | Common:1; Rare:62 | ||||
| chr19:19033437-19033776 | Common:2; Rare:106 | ||||
| chr19:19033805-19033925 | Common:1; Rare:34 | ||||
| chr19:19192083-19192268 | Common:1; Rare:59 | ||||
| chr19:19192558-19193098 | Common:3; Rare:132; Clinvar (benign):1 | ||||
| chr19:19203355-19203443 | Rare:29 | ||||
| chr19:19320467-19320874 | Common:4; Rare:157 | ||||
| chr19:19515525-19515768 | Rare:48 | ||||
| chr19:19516145-19516306 | Rare:104; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr19:19663288-19663336 | Rare:16 | ||||
| chr19:19821678-19821887 | Common:1; Rare:72 | ||||
| chr19:19900795-19900990 | Common:1; Rare:49 | ||||
| chr19:20661573-20661761 | Common:5; Rare:44 | ||||
| chr19:21082010-21082295 | Rare:62 | ||||
| chr19:23250294-23250552 | Common:2; Rare:63 |