| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:39391013-39391429 | Common:1; Rare:164 | ||||
| chr19:39406710-39406848 | Rare:52 | ||||
| chr19:39435848-39436156 | Common:6; Rare:112 | ||||
| chr19:39480732-39480934 | Common:3; Rare:107; Clinvar (pathogenic):1 | ||||
| chr19:39540149-39540426 | Common:2; Rare:53 | ||||
| chr19:39834112-39834478 | Common:3; Rare:96 | ||||
| chr19:39846330-39846469 | Common:1; Rare:63 | ||||
| chr19:39970924-39971226 | Common:4; Rare:87 | ||||
| chr19:39996958-39997090 | Common:4; Rare:45 | ||||
| chr19:40056167-40056284 | Rare:18 | ||||
| chr19:40090880-40091027 | Common:1; Rare:38 | ||||
| chr19:40348368-40348743 | Common:4; Rare:124 | ||||
| chr19:40715074-40715148 | Rare:24 | ||||
| chr19:40715758-40715968 | Common:3; Rare:41 | ||||
| chr19:40716879-40717119 | Common:1; Rare:73 |