| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:38831765-38832061 | Common:4; Rare:85; Clinvar (benign):1 | ||||
| chr19:38852305-38852674 | Rare:89 | ||||
| chr19:38899537-38900079 | Rare:162 | ||||
| chr19:38930706-38931023 | Common:3; Rare:92; Clinvar:2; Clinvar (benign):3 | ||||
| chr19:39390850-39390933 | Rare:36 | ||||
| chr19:39390991-39391452 | Common:1; Rare:179 | ||||
| chr19:39406705-39406847 | Rare:53 | ||||
| chr19:39435854-39436163 | Common:6; Rare:112 | ||||
| chr19:39445470-39445822 | Common:2; Rare:97 | ||||
| chr19:39480725-39480937 | Common:3; Rare:111; Clinvar (pathogenic):1 | ||||
| chr19:39846289-39846496 | Common:1; Rare:96 | ||||
| chr19:39970866-39971205 | Common:5; Rare:96 | ||||
| chr19:39996925-39997079 | Common:5; Rare:46 | ||||
| chr19:40056168-40056298 | Rare:18 | ||||
| chr19:40090865-40091015 | Common:1; Rare:42 |