| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:37907007-37907293 | Common:1; Rare:67 | ||||
| chr19:38224066-38224348 | Rare:78 | ||||
| chr19:38229602-38229922 | Common:1; Rare:80 | ||||
| chr19:38264253-38264585 | Common:6; Rare:85 | ||||
| chr19:38315860-38316130 | Rare:85 | ||||
| chr19:38374407-38374938 | Rare:203 | ||||
| chr19:38596082-38596336 | Rare:73 | ||||
| chr19:38618923-38619277 | Common:3; Rare:105 | ||||
| chr19:38647381-38647733 | Common:3; Rare:127 | ||||
| chr19:38831748-38832040 | Common:4; Rare:95; Clinvar (benign):1 | ||||
| chr19:38852319-38852455 | Rare:40 | ||||
| chr19:38899513-38900033 | Rare:158 | ||||
| chr19:38912176-38912309 | Common:1; Rare:41 | ||||
| chr19:38930424-38930537 | Common:1; Rare:57; Clinvar (benign):1 | ||||
| chr19:38930738-38930996 | Common:3; Rare:70; Clinvar:2; Clinvar (benign):3 |