| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:45692223-45692713 | Common:2; Rare:110 | ||||
| chr19:45730853-45730939 | Common:1; Rare:21 | ||||
| chr19:45768224-45768364 | Rare:59; Clinvar (benign):1 | ||||
| chr19:45768847-45769049 | Common:3; Rare:64; Clinvar (benign):2 | ||||
| chr19:45864186-45864326 | Common:2; Rare:32 | ||||
| chr19:45886108-45886226 | Rare:40 | ||||
| chr19:45902601-45902900 | Common:3; Rare:82 | ||||
| chr19:46382379-46382419 | Rare:5 | ||||
| chr19:46600907-46601432 | Common:6; Rare:180; Clinvar (benign):3 | ||||
| chr19:46608291-46608504 | Common:1; Rare:55; Clinvar (benign):4 | ||||
| chr19:46745776-46746071 | Common:3; Rare:63 | ||||
| chr19:46746215-46746548 | Common:4; Rare:98 | ||||
| chr19:46784650-46785054 | Common:4; Rare:104 | ||||
| chr19:46787241-46787552 | Common:1; Rare:86 | ||||
| chr19:46787879-46788121 | Common:2; Rare:48 |