| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:45406341-45406687 | Common:2; Rare:86 | ||||
| chr19:45423494-45423821 | Common:3; Rare:69; Clinvar (benign):1 | ||||
| chr19:45507228-45507508 | Common:1; Rare:72 | ||||
| chr19:45643697-45643834 | Rare:29 | ||||
| chr19:45691898-45692294 | Common:1; Rare:108 | ||||
| chr19:45692416-45692738 | Common:2; Rare:77 | ||||
| chr19:45730860-45731123 | Common:1; Rare:60 | ||||
| chr19:45769224-45769578 | Common:1; Rare:156 | ||||
| chr19:45863099-45863385 | Common:4; Rare:93 | ||||
| chr19:46023050-46023212 | Common:2; Rare:36 | ||||
| chr19:46346927-46347148 | Common:3; Rare:75 | ||||
| chr19:46471475-46471685 | Common:5; Rare:84 | ||||
| chr19:46495838-46495982 | Rare:44 | ||||
| chr19:46600903-46601436 | Common:6; Rare:183; Clinvar (benign):3 | ||||
| chr19:46745805-46746068 | Common:3; Rare:54 |