| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:39943724-39943799 | Rare:15 | ||||
| chr19:40605176-40605425 | Rare:58; Clinvar:1; Clinvar (benign):1 | ||||
| chr19:40754641-40754779 | Rare:20 | ||||
| chr19:41198573-41198754 | Common:1; Rare:49 | ||||
| chr19:41531561-41531824 | Common:1; Rare:57 | ||||
| chr19:41887837-41888085 | Common:1; Rare:64 | ||||
| chr19:41901652-41901926 | Rare:53 | ||||
| chr19:41956626-41956736 | Common:1; Rare:20 | ||||
| chr19:42286853-42287130 | Rare:94 | ||||
| chr19:42396933-42397184 | Common:1; Rare:59 | ||||
| chr19:43668957-43669018 | Common:1; Rare:15 | ||||
| chr19:44624330-44624589 | Rare:40 | ||||
| chr19:44725162-44725461 | Common:5; Rare:75 | ||||
| chr19:44746667-44746887 | Common:1; Rare:33 | ||||
| chr19:45885370-45885589 | Rare:78 |