| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:38253198-38253459 | Common:2; Rare:44 | ||||
| chr19:38264235-38264723 | Common:6; Rare:122 | ||||
| chr19:38264741-38265013 | Common:1; Rare:81 | ||||
| chr19:38647372-38647919 | Common:3; Rare:166 | ||||
| chr19:38724181-38724562 | Common:2; Rare:131; Clinvar:1; Clinvar (benign):3 | ||||
| chr19:38812840-38813252 | Common:1; Rare:98 | ||||
| chr19:38831704-38831866 | Common:3; Rare:73; Clinvar (benign):1 | ||||
| chr19:38852319-38852598 | Rare:69 | ||||
| chr19:38899511-38900018 | Rare:153 | ||||
| chr19:38930699-38930992 | Common:3; Rare:87; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr19:39342363-39342510 | Common:2; Rare:47 | ||||
| chr19:39390850-39390902 | Rare:20 | ||||
| chr19:39390985-39391002 | Rare:3 | ||||
| chr19:39391025-39391436 | Common:1; Rare:168 | ||||
| chr19:39406679-39406951 | Rare:104 |