| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:45584774-45585022 | Common:4; Rare:97; Clinvar:1; Clinvar (benign):4 | ||||
| chr19:46346941-46347112 | Common:3; Rare:53 | ||||
| chr19:46600913-46601415 | Common:5; Rare:173; Clinvar (benign):1 | ||||
| chr19:46608290-46608487 | Common:1; Rare:53; Clinvar (benign):4 | ||||
| chr19:46745980-46746068 | Common:3; Rare:25 | ||||
| chr19:46787260-46787531 | Common:1; Rare:74 | ||||
| chr19:46788510-46788627 | Rare:28 | ||||
| chr19:47113137-47113429 | Common:1; Rare:77 | ||||
| chr19:47130639-47130978 | Common:1; Rare:112 | ||||
| chr19:47256459-47256577 | Rare:46 | ||||
| chr19:47484182-47484386 | Common:2; Rare:66 | ||||
| chr19:48170324-48170703 | Common:2; Rare:93 | ||||
| chr19:48325261-48325610 | Common:2; Rare:77 | ||||
| chr19:48390848-48390949 | Rare:13 | ||||
| chr19:48445890-48446035 | Common:1; Rare:57 |