| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:47484164-47484386 | Common:2; Rare:75 | ||||
| chr19:48170273-48170704 | Common:2; Rare:116 | ||||
| chr19:48445889-48446005 | Rare:44 | ||||
| chr19:48619147-48619654 | Common:1; Rare:161 | ||||
| chr19:48993281-48993535 | Common:3; Rare:111; Clinvar:2; Clinvar (benign):2 | ||||
| chr19:49361509-49361726 | Rare:39 | ||||
| chr19:49362386-49362498 | Rare:35 | ||||
| chr19:49453093-49453311 | Common:1; Rare:70 | ||||
| chr19:49580536-49580682 | Rare:46 | ||||
| chr19:49639965-49640523 | Common:1; Rare:174; Clinvar:3; Clinvar (benign):1 | ||||
| chr19:49665761-49666029 | Common:3; Rare:132; Clinvar (pathogenic):1 | ||||
| chr19:49851055-49851184 | Common:1; Rare:51 | ||||
| chr19:49876582-49876979 | Common:1; Rare:124 | ||||
| chr19:49877273-49877724 | Common:1; Rare:116 | ||||
| chr19:49877867-49878196 | Common:3; Rare:108 |