| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:38724196-38724565 | Common:2; Rare:126; Clinvar:1; Clinvar (benign):3 | ||||
| chr19:38727864-38728022 | Rare:55; Clinvar (benign):2 | ||||
| chr19:38815583-38815995 | Common:2; Rare:145; Clinvar (benign):1 | ||||
| chr19:38899531-38900084 | Rare:166 | ||||
| chr19:38930742-38930996 | Common:3; Rare:67; Clinvar:2; Clinvar (benign):3 | ||||
| chr19:38975653-38975887 | Common:1; Rare:60 | ||||
| chr19:39390817-39390932 | Rare:47; Clinvar:1 | ||||
| chr19:39390974-39391442 | Common:1; Rare:181 | ||||
| chr19:39406699-39406935 | Rare:95 | ||||
| chr19:39407009-39407347 | Rare:69 | ||||
| chr19:39412306-39412710 | Common:3; Rare:156 | ||||
| chr19:39412826-39413003 | Common:1; Rare:39 | ||||
| chr19:39435846-39436154 | Common:6; Rare:111 | ||||
| chr19:39445485-39445813 | Common:2; Rare:87 | ||||
| chr19:39480731-39480931 | Common:3; Rare:108; Clinvar (pathogenic):1 |