| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:39480664-39480997 | Common:5; Rare:151; Clinvar (pathogenic):1 | ||||
| chr19:39532141-39532416 | Rare:57 | ||||
| chr19:39532747-39532990 | Rare:99 | ||||
| chr19:39540053-39540378 | Common:3; Rare:87 | ||||
| chr19:39833436-39833763 | Common:2; Rare:102 | ||||
| chr19:39834067-39834314 | Rare:69 | ||||
| chr19:39846260-39846709 | Common:1; Rare:166 | ||||
| chr19:39970418-39970712 | Common:1; Rare:45 | ||||
| chr19:39970746-39971244 | Common:7; Rare:131 | ||||
| chr19:39996830-39997254 | Common:5; Rare:91 | ||||
| chr19:39997267-39997501 | Rare:39 | ||||
| chr19:40056105-40056544 | Common:1; Rare:76 | ||||
| chr19:40090482-40090727 | Common:2; Rare:49 | ||||
| chr19:40090798-40091120 | Common:1; Rare:81 | ||||
| chr19:40191303-40191516 | Common:2; Rare:50 |