| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:45370552-45370799 | Common:2; Rare:73 | ||||
| chr19:45406355-45406649 | Common:1; Rare:64 | ||||
| chr19:45423822-45424012 | Common:2; Rare:39 | ||||
| chr19:45507226-45507508 | Common:1; Rare:72 | ||||
| chr19:45691904-45692113 | Rare:69 | ||||
| chr19:45730857-45731047 | Common:1; Rare:40 | ||||
| chr19:46296841-46297062 | Common:4; Rare:80 | ||||
| chr19:46298120-46298439 | Common:5; Rare:76 | ||||
| chr19:46346941-46347153 | Common:3; Rare:74 | ||||
| chr19:46471485-46471626 | Common:5; Rare:54 | ||||
| chr19:46600903-46601425 | Common:6; Rare:179; Clinvar (benign):2 | ||||
| chr19:47112154-47112648 | Common:2; Rare:159 | ||||
| chr19:47130651-47130967 | Common:1; Rare:106 | ||||
| chr19:47256460-47256568 | Rare:39 | ||||
| chr19:47349088-47349379 | Rare:80 |