| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:38850406-38850690 | Common:1; Rare:92 | ||||
| chr19:38930722-38930996 | Common:3; Rare:79; Clinvar:2; Clinvar (benign):3 | ||||
| chr19:39125530-39125805 | Rare:64 | ||||
| chr19:39335986-39336185 | Rare:54 | ||||
| chr19:39390850-39390897 | Rare:18 | ||||
| chr19:39391005-39391420 | Common:1; Rare:159 | ||||
| chr19:39406698-39406852 | Rare:57 | ||||
| chr19:39435882-39436174 | Common:5; Rare:115 | ||||
| chr19:39445442-39445810 | Common:2; Rare:110 | ||||
| chr19:39480725-39480919 | Common:3; Rare:105; Clinvar (pathogenic):1 | ||||
| chr19:39846308-39846483 | Common:1; Rare:82 | ||||
| chr19:39970859-39971223 | Common:5; Rare:104 | ||||
| chr19:39996915-39997070 | Common:5; Rare:43 | ||||
| chr19:40056157-40056243 | Rare:14 | ||||
| chr19:40090886-40091011 | Common:1; Rare:34 |