| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:40777910-40778262 | Common:1; Rare:96 | ||||
| chr19:40799101-40799242 | Common:4; Rare:52 | ||||
| chr19:41219045-41219238 | Rare:33 | ||||
| chr19:41262326-41262598 | Rare:49 | ||||
| chr19:41884181-41884452 | Rare:71 | ||||
| chr19:41959282-41959459 | Common:1; Rare:57 | ||||
| chr19:42075766-42076199 | Common:5; Rare:127 | ||||
| chr19:42217696-42217910 | Rare:79 | ||||
| chr19:42268228-42268570 | Rare:69 | ||||
| chr19:42302286-42302656 | Rare:109 | ||||
| chr19:42302706-42302931 | Common:3; Rare:34 | ||||
| chr19:42325370-42325670 | Rare:87 | ||||
| chr19:42442860-42443030 | Common:3; Rare:30 | ||||
| chr19:43504101-43504343 | Common:6; Rare:77 | ||||
| chr19:43527181-43527276 | Common:4; Rare:44; Clinvar:2; Clinvar (benign):6; Clinvar (pathogenic):1 |