| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:10353219-10353482 | Common:2; Rare:46 | ||||
| chr19:10380449-10380825 | Common:12; Rare:113; Clinvar:5 | ||||
| chr19:10395085-10395291 | Rare:61 | ||||
| chr19:10568972-10569216 | Common:2; Rare:64 | ||||
| chr19:10718367-10718570 | Common:1; Rare:43; Clinvar:2 | ||||
| chr19:10796076-10796312 | Rare:61; Clinvar:1; Clinvar (benign):4 | ||||
| chr19:10835777-10835956 | Rare:53 | ||||
| chr19:10836191-10836675 | Common:3; Rare:130 | ||||
| chr19:10928551-10928795 | Common:1; Rare:68 | ||||
| chr19:10960680-10961085 | Common:4; Rare:164 | ||||
| chr19:11089377-11089533 | Rare:33; Clinvar:6; Clinvar (pathogenic):1 | ||||
| chr19:11090334-11090590 | Common:2; Rare:71 | ||||
| chr19:11155778-11156058 | Common:3; Rare:64 | ||||
| chr19:11197504-11197687 | Common:1; Rare:59 | ||||
| chr19:11374660-11374745 | Common:1; Rare:36 |