| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:48993553-48993905 | Common:5; Rare:90 | ||||
| chr19:49085130-49085492 | Common:3; Rare:145 | ||||
| chr19:49114053-49114402 | Common:4; Rare:88 | ||||
| chr19:49335303-49335462 | Common:1; Rare:29 | ||||
| chr19:49362347-49362473 | Rare:33 | ||||
| chr19:49451711-49451851 | Common:1; Rare:34 | ||||
| chr19:49453480-49453560 | Rare:23 | ||||
| chr19:49496138-49496470 | Common:1; Rare:114 | ||||
| chr19:49513087-49513403 | Common:1; Rare:71 | ||||
| chr19:49580528-49580619 | Rare:32 | ||||
| chr19:49641834-49642034 | Rare:56 | ||||
| chr19:49665600-49666023 | Common:6; Rare:197; Clinvar (pathogenic):1 | ||||
| chr19:49690980-49691138 | Rare:36 | ||||
| chr19:49808816-49809019 | Common:2; Rare:62 | ||||
| chr19:49813193-49813347 | Rare:64 |