| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:10403383-10403743 | Rare:134 | ||||
| chr19:10403864-10403923 | Rare:20 | ||||
| chr19:10502696-10502985 | Rare:81 | ||||
| chr19:10565952-10566127 | Common:2; Rare:68 | ||||
| chr19:10568972-10569230 | Common:2; Rare:67 | ||||
| chr19:10836199-10836666 | Common:3; Rare:123 | ||||
| chr19:10928573-10928882 | Common:2; Rare:106 | ||||
| chr19:10960689-10961110 | Common:3; Rare:163 | ||||
| chr19:11089295-11089516 | Rare:38; Clinvar:9; Clinvar (pathogenic):1 | ||||
| chr19:11155759-11156038 | Common:3; Rare:67 | ||||
| chr19:11197504-11197687 | Common:1; Rare:59 | ||||
| chr19:11374889-11375239 | Common:1; Rare:108 | ||||
| chr19:11418552-11418680 | Rare:31 | ||||
| chr19:11419286-11419450 | Rare:32 | ||||
| chr19:11435150-11435443 | Common:2; Rare:74 |