| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:9818788-9818888 | Rare:42 | ||||
| chr19:9827808-9828000 | Common:1; Rare:69 | ||||
| chr19:9835013-9835363 | Rare:142 | ||||
| chr19:9936316-9936635 | Common:5; Rare:106 | ||||
| chr19:10315715-10316044 | Common:7; Rare:151; Clinvar (benign):12 | ||||
| chr19:10333508-10333709 | Rare:66 | ||||
| chr19:10380487-10380824 | Common:12; Rare:98; Clinvar:5 | ||||
| chr19:10403424-10403929 | Rare:169 | ||||
| chr19:10565952-10566216 | Common:2; Rare:92 | ||||
| chr19:10568961-10569223 | Common:2; Rare:68 | ||||
| chr19:10836191-10836570 | Common:2; Rare:102 | ||||
| chr19:10928574-10928795 | Common:1; Rare:62 | ||||
| chr19:11089295-11089533 | Rare:44; Clinvar:10; Clinvar (pathogenic):1 | ||||
| chr19:11155706-11156061 | Common:3; Rare:93 | ||||
| chr19:11197510-11197641 | Common:1; Rare:39 |