| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:42217671-42217881 | Rare:80 | ||||
| chr19:42220112-42220341 | Common:2; Rare:64 | ||||
| chr19:42268251-42268570 | Rare:63 | ||||
| chr19:42302318-42302458 | Rare:46 | ||||
| chr19:42528437-42528604 | Common:2; Rare:38 | ||||
| chr19:43186495-43186710 | Common:4; Rare:67 | ||||
| chr19:43205587-43205651 | Common:4; Rare:18 | ||||
| chr19:43464322-43464548 | Rare:81 | ||||
| chr19:43465491-43465825 | Common:1; Rare:110 | ||||
| chr19:43527133-43527310 | Common:5; Rare:67; Clinvar:4; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
| chr19:43553415-43553640 | Common:2; Rare:75; Clinvar:1 | ||||
| chr19:43575433-43575746 | Common:2; Rare:97 | ||||
| chr19:43576551-43576807 | Common:1; Rare:46 | ||||
| chr19:43596118-43596438 | Common:2; Rare:99 | ||||
| chr19:43670129-43670305 | Common:2; Rare:41 |