| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:19033814-19033916 | Common:1; Rare:27 | ||||
| chr19:19192092-19192268 | Common:1; Rare:57 | ||||
| chr19:19192587-19192968 | Common:2; Rare:99 | ||||
| chr19:19320467-19320865 | Common:4; Rare:150 | ||||
| chr19:19385851-19386048 | Rare:73 | ||||
| chr19:19516157-19516302 | Rare:87; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr19:19643575-19643736 | Common:3; Rare:52 | ||||
| chr19:19663529-19663723 | Rare:71 | ||||
| chr19:19668667-19668849 | Common:1; Rare:52 | ||||
| chr19:19821660-19821905 | Common:1; Rare:81 | ||||
| chr19:21329279-21329440 | Common:1; Rare:33 | ||||
| chr19:21396943-21397183 | Rare:64 | ||||
| chr19:23395369-23395627 | Common:1; Rare:85 | ||||
| chr19:29213111-29213298 | Common:3; Rare:61 | ||||
| chr19:29606186-29606319 | Rare:44 |