| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:38736946-38737124 | Common:3; Rare:22 | ||||
| chr19:38831787-38832076 | Common:3; Rare:78 | ||||
| chr19:38841867-38842063 | Rare:51 | ||||
| chr19:38842209-38842253 | Rare:10 | ||||
| chr19:38849913-38850069 | Common:1; Rare:55 | ||||
| chr19:38852335-38852482 | Rare:36 | ||||
| chr19:38878246-38878324 | Rare:13 | ||||
| chr19:38899508-38900030 | Rare:155 | ||||
| chr19:38930723-38930969 | Common:2; Rare:66; Clinvar:2; Clinvar (benign):3 | ||||
| chr19:39390600-39390807 | Rare:48 | ||||
| chr19:39390865-39391420 | Common:1; Rare:207 | ||||
| chr19:39406341-39406407 | Rare:15 | ||||
| chr19:39406710-39406873 | Rare:66 | ||||
| chr19:39407582-39407883 | Common:1; Rare:84 | ||||
| chr19:39435673-39435998 | Common:4; Rare:149 |