| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:50309554-50309732 | Common:1; Rare:64; Clinvar:4; Clinvar (benign):4 | ||||
| chr19:51594347-51594602 | Common:2; Rare:69 | ||||
| chr19:52601173-52601317 | Common:3; Rare:48 | ||||
| chr19:52616891-52617050 | Common:2; Rare:45 | ||||
| chr19:54124317-54124554 | Common:1; Rare:73; Clinvar (benign):1 | ||||
| chr19:54148424-54148691 | Common:2; Rare:109 | ||||
| chr19:55185497-55185823 | Common:2; Rare:94 | ||||
| chr19:55185888-55186078 | Common:1; Rare:58 | ||||
| chr19:55257994-55258114 | Common:2; Rare:36 | ||||
| chr19:55321559-55321709 | Common:1; Rare:16 | ||||
| chr19:55636407-55636608 | Common:3; Rare:49 | ||||
| chr19:55639477-55639632 | Rare:15 | ||||
| chr19:55668386-55668687 | Common:1; Rare:94 | ||||
| chr19:55688649-55688993 | Common:3; Rare:94 | ||||
| chr19:57786382-57786655 | Common:1; Rare:60 |