| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:38852370-38852383 | |||||
| chr19:38899504-38900033 | Rare:160 | ||||
| chr19:38930720-38931002 | Common:3; Rare:83; Clinvar:2; Clinvar (benign):3 | ||||
| chr19:38975724-38975852 | Common:1; Rare:33 | ||||
| chr19:39342410-39342485 | Common:2; Rare:27 | ||||
| chr19:39391025-39391425 | Common:1; Rare:161 | ||||
| chr19:39406684-39406928 | Rare:93 | ||||
| chr19:39435846-39436160 | Common:6; Rare:115 | ||||
| chr19:39846317-39846473 | Common:1; Rare:72 | ||||
| chr19:39970925-39971196 | Common:4; Rare:75 | ||||
| chr19:39996956-39997101 | Common:4; Rare:50 | ||||
| chr19:40056135-40056243 | Rare:15 | ||||
| chr19:40090871-40090999 | Common:1; Rare:35 | ||||
| chr19:40285197-40285622 | Common:3; Rare:141 | ||||
| chr19:40348352-40348740 | Common:4; Rare:127 |