| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:38930732-38930992 | Common:3; Rare:73; Clinvar:2; Clinvar (benign):3 | ||||
| chr19:39390827-39391488 | Common:1; Rare:253; Clinvar:1 | ||||
| chr19:39406695-39406913 | Rare:86 | ||||
| chr19:39412317-39412587 | Common:2; Rare:121 | ||||
| chr19:39480575-39480888 | Common:3; Rare:146; Clinvar (pathogenic):1 | ||||
| chr19:39846317-39846473 | Common:1; Rare:72 | ||||
| chr19:39970948-39971205 | Common:3; Rare:70 | ||||
| chr19:39996935-39997074 | Common:5; Rare:40 | ||||
| chr19:40056135-40056330 | Rare:28 | ||||
| chr19:40090871-40090999 | Common:1; Rare:35 | ||||
| chr19:40285233-40285623 | Common:3; Rare:133 | ||||
| chr19:40348388-40348724 | Common:4; Rare:110 | ||||
| chr19:40413365-40413543 | Rare:50 | ||||
| chr19:40444287-40444499 | Common:3; Rare:68 | ||||
| chr19:40465700-40466105 | Common:3; Rare:125 |