| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:7501092-7501290 | Common:2; Rare:78 | ||||
| chr19:7515879-7515944 | Rare:14 | ||||
| chr19:7515946-7516199 | Rare:61 | ||||
| chr19:7516443-7516488 | Common:1; Rare:14 | ||||
| chr19:7522408-7522708 | Common:2; Rare:101; Clinvar:2 | ||||
| chr19:7533514-7533601 | Rare:33 | ||||
| chr19:7533650-7533692 | Rare:13 | ||||
| chr19:7534012-7534262 | Common:4; Rare:67; Clinvar (benign):2 | ||||
| chr19:7534650-7534798 | Rare:21 | ||||
| chr19:7535534-7535747 | Common:3; Rare:72; Clinvar:2 | ||||
| chr19:7629463-7629871 | Common:7; Rare:152; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr19:7636975-7637217 | Common:2; Rare:72; Clinvar:1; Clinvar (benign):1 | ||||
| chr19:7680666-7680921 | Common:3; Rare:85 | ||||
| chr19:7829944-7830280 | Common:2; Rare:92 | ||||
| chr19:7874440-7874503 | Rare:18 |