| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:1269187-1269339 | Common:1; Rare:59 | ||||
| chr19:1354786-1355002 | Common:2; Rare:89 | ||||
| chr19:1438280-1438433 | Rare:61 | ||||
| chr19:1605390-1605566 | Common:3; Rare:72 | ||||
| chr19:1905194-1905417 | Common:4; Rare:90 | ||||
| chr19:2269241-2269572 | Common:2; Rare:144 | ||||
| chr19:2328559-2328703 | Common:2; Rare:70 | ||||
| chr19:2783250-2783493 | Rare:87 | ||||
| chr19:2841240-2841539 | Common:2; Rare:93 | ||||
| chr19:2900642-2900966 | Common:10; Rare:125 | ||||
| chr19:2944917-2945181 | Common:5; Rare:91 | ||||
| chr19:3500649-3500961 | Common:4; Rare:80 | ||||
| chr19:3576847-3576941 | Rare:42 | ||||
| chr19:3971044-3971377 | Common:2; Rare:111 | ||||
| chr19:3982805-3983194 | Common:5; Rare:139; Clinvar:1; Clinvar (benign):3 |