| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:10339618-10339710 | Rare:30 | ||||
| chr19:10380503-10380861 | Common:13; Rare:103; Clinvar:5 | ||||
| chr19:10419526-10419695 | Rare:40 | ||||
| chr19:10502713-10502946 | Rare:63 | ||||
| chr19:10568974-10569325 | Common:2; Rare:85 | ||||
| chr19:10602302-10602531 | Rare:69 | ||||
| chr19:10653839-10653895 | Rare:20 | ||||
| chr19:10654119-10654379 | Common:4; Rare:126 | ||||
| chr19:10777208-10777492 | Rare:51 | ||||
| chr19:10836200-10836261 | Rare:19 | ||||
| chr19:10928594-10928724 | Common:1; Rare:32 | ||||
| chr19:10960668-10961164 | Common:6; Rare:190; Clinvar (benign):2 | ||||
| chr19:11089269-11089499 | Rare:31; Clinvar:8; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr19:11155756-11156095 | Common:3; Rare:90 | ||||
| chr19:11197504-11197676 | Common:1; Rare:56 |