| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:46346931-46347181 | Common:3; Rare:88 | ||||
| chr19:46413378-46413773 | Common:1; Rare:111 | ||||
| chr19:46471419-46471737 | Common:9; Rare:117 | ||||
| chr19:46600913-46601076 | Common:2; Rare:66 | ||||
| chr19:46601194-46601425 | Common:4; Rare:67; Clinvar (benign):2 | ||||
| chr19:46608278-46608487 | Common:1; Rare:54; Clinvar (benign):4 | ||||
| chr19:46661025-46661230 | Rare:52 | ||||
| chr19:46745895-46746066 | Common:3; Rare:36 | ||||
| chr19:46746306-46746560 | Common:4; Rare:78 | ||||
| chr19:46788563-46788666 | Rare:26 | ||||
| chr19:46850245-46850393 | Rare:21 | ||||
| chr19:47112146-47112603 | Common:2; Rare:153 | ||||
| chr19:47130615-47130964 | Common:1; Rare:111 | ||||
| chr19:47256472-47256577 | Rare:39 | ||||
| chr19:47349045-47349387 | Common:1; Rare:102 |