| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:45902611-45902935 | Common:3; Rare:95 | ||||
| chr19:46298120-46298443 | Common:5; Rare:77 | ||||
| chr19:46346941-46347204 | Common:3; Rare:92 | ||||
| chr19:46601196-46601409 | Common:3; Rare:63; Clinvar (benign):1 | ||||
| chr19:46714254-46714491 | Common:2; Rare:49 | ||||
| chr19:46745756-46746068 | Common:3; Rare:64 | ||||
| chr19:46787421-46787531 | Rare:35 | ||||
| chr19:47112146-47112344 | Rare:56 | ||||
| chr19:47113097-47113429 | Common:2; Rare:88 | ||||
| chr19:47256472-47256577 | Rare:39 | ||||
| chr19:47274127-47274435 | Common:3; Rare:91 | ||||
| chr19:47349073-47349387 | Rare:90 | ||||
| chr19:47484250-47484302 | Rare:13 | ||||
| chr19:47512767-47512885 | Rare:21 | ||||
| chr19:47608153-47608195 | Rare:12 |