| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:45862601-45862888 | Common:1; Rare:84 | ||||
| chr19:45863053-45863442 | Common:5; Rare:120 | ||||
| chr19:45864107-45864358 | Common:2; Rare:56 | ||||
| chr19:45885841-45885984 | Rare:27 | ||||
| chr19:45886047-45886298 | Common:4; Rare:90 | ||||
| chr19:45886411-45886685 | Common:6; Rare:47 | ||||
| chr19:45902496-45903003 | Common:5; Rare:150 | ||||
| chr19:45994974-45995532 | Common:4; Rare:220 | ||||
| chr19:46346834-46347148 | Common:3; Rare:110 | ||||
| chr19:46347432-46347574 | Rare:30 | ||||
| chr19:46600528-46600709 | Rare:39 | ||||
| chr19:46600855-46601416 | Common:5; Rare:191; Clinvar (benign):1 | ||||
| chr19:46625029-46625439 | Common:2; Rare:75 | ||||
| chr19:46634218-46634543 | Common:2; Rare:54 | ||||
| chr19:46713623-46713935 | Common:2; Rare:73 |