| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:19170230-19170426 | Common:2; Rare:51 | ||||
| chr19:19192068-19192366 | Common:3; Rare:82; Clinvar (benign):1 | ||||
| chr19:19192502-19192974 | Common:2; Rare:122 | ||||
| chr19:19203336-19203566 | Rare:65 | ||||
| chr19:19273209-19273309 | Rare:30 | ||||
| chr19:19320408-19320931 | Common:7; Rare:230 | ||||
| chr19:19321056-19321106 | Rare:10 | ||||
| chr19:19321342-19321480 | Common:1; Rare:29 | ||||
| chr19:19385212-19385892 | Common:1; Rare:190 | ||||
| chr19:19385925-19386182 | Rare:76 | ||||
| chr19:19405352-19405877 | Common:4; Rare:159 | ||||
| chr19:19464444-19464584 | Common:1; Rare:27 | ||||
| chr19:19515410-19515797 | Rare:93 | ||||
| chr19:19516076-19516342 | Rare:155; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr19:19516455-19516473 | Rare:6 |