| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:9827823-9827982 | Common:1; Rare:58 | ||||
| chr19:10231260-10231590 | Common:2; Rare:69 | ||||
| chr19:10333509-10333739 | Rare:76 | ||||
| chr19:10380487-10380820 | Common:12; Rare:96; Clinvar:5 | ||||
| chr19:10403383-10403778 | Rare:142 | ||||
| chr19:10565966-10566263 | Common:2; Rare:97 | ||||
| chr19:10836200-10836229 | Rare:8 | ||||
| chr19:10836258-10836571 | Common:2; Rare:79 | ||||
| chr19:10928526-10928795 | Common:1; Rare:74 | ||||
| chr19:10960706-10961164 | Common:3; Rare:165; Clinvar (benign):2 | ||||
| chr19:11089295-11089533 | Rare:44; Clinvar:10; Clinvar (pathogenic):1 | ||||
| chr19:11090348-11090574 | Common:2; Rare:60 | ||||
| chr19:11197504-11197622 | Common:1; Rare:32 | ||||
| chr19:11435180-11435441 | Common:2; Rare:68 | ||||
| chr19:11529086-11529287 | Rare:39 |