| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:74148313-74148568 | Common:2; Rare:92 | ||||
| chr18:74496029-74496371 | Common:4; Rare:106 | ||||
| chr18:79988349-79988651 | Common:3; Rare:107; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr19:507464-507503 | Rare:13 | ||||
| chr19:572237-572629 | Common:3; Rare:193 | ||||
| chr19:633520-633745 | Common:8; Rare:99 | ||||
| chr19:663154-663430 | Common:2; Rare:108 | ||||
| chr19:984207-984348 | Common:3; Rare:52 | ||||
| chr19:1103801-1104120 | Common:4; Rare:134 | ||||
| chr19:1169202-1169294 | Common:1; Rare:20 | ||||
| chr19:1354850-1355002 | Rare:56 | ||||
| chr19:1479161-1479330 | Common:1; Rare:66 | ||||
| chr19:1605405-1605657 | Common:3; Rare:99 | ||||
| chr19:2328538-2328703 | Common:2; Rare:80 | ||||
| chr19:2783250-2783448 | Rare:71 |