| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:9818811-9818887 | Rare:32 | ||||
| chr19:9827814-9827982 | Common:1; Rare:63 | ||||
| chr19:10315851-10316036 | Common:4; Rare:88; Clinvar (benign):7 | ||||
| chr19:10333517-10333733 | Rare:73 | ||||
| chr19:10403451-10403937 | Rare:169 | ||||
| chr19:10568965-10569221 | Common:2; Rare:67 | ||||
| chr19:10653817-10653881 | Rare:27 | ||||
| chr19:10960717-10961087 | Common:3; Rare:147 | ||||
| chr19:11089300-11089516 | Rare:37; Clinvar:9; Clinvar (pathogenic):1 | ||||
| chr19:11155772-11156086 | Common:3; Rare:79 | ||||
| chr19:11197504-11197622 | Common:1; Rare:32 | ||||
| chr19:11374519-11374732 | Common:1; Rare:66 | ||||
| chr19:11435180-11435440 | Common:2; Rare:68 | ||||
| chr19:11559210-11559399 | Common:1; Rare:55 | ||||
| chr19:11597309-11597520 | Rare:65 |