| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:48954666-48954931 | Common:1; Rare:99 | ||||
| chr19:48965240-48965916 | Common:1; Rare:232; Clinvar:6; Clinvar (benign):1; Clinvar (pathogenic):8 | ||||
| chr19:48993253-48993495 | Common:2; Rare:114; Clinvar:3; Clinvar (benign):2 | ||||
| chr19:48993553-48993922 | Common:5; Rare:96 | ||||
| chr19:49085096-49085492 | Common:3; Rare:154 | ||||
| chr19:49362375-49362471 | Rare:25 | ||||
| chr19:49453019-49453311 | Common:2; Rare:90 | ||||
| chr19:49453473-49453612 | Rare:39 | ||||
| chr19:49474087-49474272 | Common:1; Rare:49 | ||||
| chr19:49527861-49528032 | Common:3; Rare:53 | ||||
| chr19:49580534-49580686 | Rare:47 | ||||
| chr19:49665732-49666039 | Common:3; Rare:140; Clinvar (pathogenic):1 | ||||
| chr19:49690976-49691142 | Rare:37 | ||||
| chr19:49813258-49813307 | Rare:20 | ||||
| chr19:49817296-49817625 | Common:3; Rare:68 |