| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:10315720-10316044 | Common:7; Rare:150; Clinvar (benign):12 | ||||
| chr19:10333484-10333744 | Common:1; Rare:89 | ||||
| chr19:10380487-10380854 | Common:13; Rare:111; Clinvar:5 | ||||
| chr19:10403383-10403965 | Rare:185 | ||||
| chr19:10452750-10453098 | Rare:78 | ||||
| chr19:10502686-10502795 | Rare:33 | ||||
| chr19:10543765-10543909 | Common:1; Rare:38 | ||||
| chr19:10565986-10566233 | Common:2; Rare:77 | ||||
| chr19:10568946-10569230 | Common:2; Rare:75 | ||||
| chr19:10602282-10602544 | Common:1; Rare:78 | ||||
| chr19:10654686-10655089 | Common:6; Rare:167 | ||||
| chr19:10655762-10655845 | Rare:23 | ||||
| chr19:10701384-10701518 | Rare:60 | ||||
| chr19:10712837-10712914 | Rare:20 | ||||
| chr19:10836199-10836274 | Rare:20 |