| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:42396806-42397325 | Common:3; Rare:117 | ||||
| chr19:42401858-42402018 | Common:1; Rare:59; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr19:42468460-42468644 | Rare:39 | ||||
| chr19:43475257-43475574 | Common:2; Rare:135 | ||||
| chr19:43562798-43562843 | Common:1; Rare:11 | ||||
| chr19:43562846-43563070 | Common:1; Rare:48 | ||||
| chr19:43564959-43565193 | Rare:41 | ||||
| chr19:43594860-43595007 | Rare:57 | ||||
| chr19:43635067-43635406 | Rare:71 | ||||
| chr19:43701455-43701613 | Rare:27 | ||||
| chr19:43755578-43755670 | Common:1; Rare:27 | ||||
| chr19:43785426-43785580 | Common:1; Rare:31 | ||||
| chr19:43984799-43984897 | Common:1; Rare:15 | ||||
| chr19:44002133-44002364 | Common:1; Rare:37 | ||||
| chr19:44213184-44213235 | Rare:12 |