| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:39435848-39436282 | Common:57; Rare:956 | ||||
| chr19:39445320-39445822 | Common:29; Rare:815 | ||||
| chr19:39457374-39457934 | Common:3; Rare:237 | ||||
| chr19:39479852-39480345 | Common:10; Rare:200 | ||||
| chr19:39480445-39480976 | Common:20; Rare:1204; Clinvar (pathogenic):6 | ||||
| chr19:39481216-39481399 | Common:1; Rare:53 | ||||
| chr19:39481631-39482056 | Rare:213 | ||||
| chr19:39498618-39498752 | Rare:30 | ||||
| chr19:39532150-39532550 | Common:1; Rare:102 | ||||
| chr19:39532729-39533150 | Common:4; Rare:343 | ||||
| chr19:39540067-39540511 | Common:6; Rare:207 | ||||
| chr19:39833420-39833920 | Common:5; Rare:349 | ||||
| chr19:39834056-39834456 | Common:5; Rare:316 | ||||
| chr19:39839671-39840463 | Common:14; Rare:338 | ||||
| chr19:39840413-39840621 | Rare:72 |