| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:45038966-45039094 | Rare:42 | ||||
| chr19:45091579-45091792 | Common:2; Rare:55 | ||||
| chr19:45370553-45370747 | Common:2; Rare:61 | ||||
| chr19:45406362-45406654 | Common:1; Rare:64 | ||||
| chr19:45507228-45507508 | Common:1; Rare:72 | ||||
| chr19:45584774-45585054 | Common:4; Rare:106; Clinvar:1; Clinvar (benign):4 | ||||
| chr19:45692536-45692706 | Rare:40 | ||||
| chr19:45730869-45731026 | Common:1; Rare:34 | ||||
| chr19:46346918-46347124 | Common:3; Rare:63 | ||||
| chr19:46471480-46471626 | Common:5; Rare:55 | ||||
| chr19:46495836-46496028 | Rare:56 | ||||
| chr19:46600913-46601434 | Common:6; Rare:179; Clinvar (benign):3 | ||||
| chr19:46746447-46746628 | Common:2; Rare:50 | ||||
| chr19:47112146-47112356 | Rare:62 | ||||
| chr19:47113064-47113308 | Common:1; Rare:68 |