| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:51339709-51340126 | Common:1; Rare:90 | ||||
| chr19:51340156-51340315 | Rare:50 | ||||
| chr19:51365553-51365919 | Common:3; Rare:57 | ||||
| chr19:51366282-51366732 | Common:8; Rare:126; Clinvar (benign):2 | ||||
| chr19:51366833-51367150 | Common:3; Rare:69 | ||||
| chr19:51367452-51367919 | Common:3; Rare:147 | ||||
| chr19:51367938-51367954 | Common:1; Rare:4 | ||||
| chr19:51368066-51368189 | Common:1; Rare:37 | ||||
| chr19:51531736-51532056 | Common:9; Rare:55 | ||||
| chr19:51571110-51571317 | Common:5; Rare:59 | ||||
| chr19:51887547-51887629 | Rare:15 | ||||
| chr19:51887808-51888142 | Rare:104 | ||||
| chr19:51926731-51926881 | Common:1; Rare:29 | ||||
| chr19:51986800-51986999 | Common:1; Rare:54 | ||||
| chr19:52008033-52008488 | Common:2; Rare:99 |