| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:49157483-49157855 | Common:2; Rare:105; Clinvar:1 | ||||
| chr19:49359910-49360237 | Common:1; Rare:101 | ||||
| chr19:49361491-49361601 | Rare:20 | ||||
| chr19:49362306-49362517 | Rare:54 | ||||
| chr19:49451735-49451925 | Common:2; Rare:45 | ||||
| chr19:49453089-49453311 | Common:1; Rare:71 | ||||
| chr19:49453450-49453639 | Common:1; Rare:62 | ||||
| chr19:49475338-49475489 | Rare:36 | ||||
| chr19:49496113-49496500 | Common:1; Rare:138 | ||||
| chr19:49513115-49513440 | Common:1; Rare:73 | ||||
| chr19:49513737-49513863 | Common:3; Rare:37 | ||||
| chr19:49527766-49528349 | Common:5; Rare:142 | ||||
| chr19:49580518-49580650 | Rare:47 | ||||
| chr19:49639949-49640520 | Common:1; Rare:177; Clinvar:4; Clinvar (benign):1 | ||||
| chr19:49641831-49642271 | Rare:122 |