| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:9835013-9835397 | Rare:154 | ||||
| chr19:10116868-10117152 | Rare:83 | ||||
| chr19:10119656-10119997 | Common:2; Rare:125 | ||||
| chr19:10231271-10231343 | Common:1; Rare:22 | ||||
| chr19:10333504-10333715 | Rare:69 | ||||
| chr19:10503313-10503410 | Rare:24 | ||||
| chr19:10653833-10653887 | Rare:21 | ||||
| chr19:10836184-10836261 | Rare:25 | ||||
| chr19:10928557-10928806 | Common:2; Rare:72 | ||||
| chr19:10960680-10961080 | Common:4; Rare:164 | ||||
| chr19:11089307-11089533 | Rare:42; Clinvar:10; Clinvar (pathogenic):1 | ||||
| chr19:11090338-11090602 | Common:2; Rare:78 | ||||
| chr19:11197483-11197676 | Common:1; Rare:59 | ||||
| chr19:11197735-11198013 | Common:2; Rare:76 | ||||
| chr19:11203407-11203765 | Rare:86 |