| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:39406706-39406926 | Rare:91 | ||||
| chr19:39407035-39407106 | Rare:12 | ||||
| chr19:39407396-39407962 | Common:1; Rare:155 | ||||
| chr19:39412856-39412909 | Rare:6 | ||||
| chr19:39435846-39436154 | Common:6; Rare:111 | ||||
| chr19:39480716-39480912 | Common:3; Rare:106; Clinvar (pathogenic):1 | ||||
| chr19:39540152-39540357 | Common:1; Rare:47 | ||||
| chr19:39846309-39846468 | Common:1; Rare:74 | ||||
| chr19:39970943-39971214 | Common:4; Rare:74 | ||||
| chr19:39996935-39997118 | Common:5; Rare:59 | ||||
| chr19:40056148-40056260 | Rare:15 | ||||
| chr19:40090865-40090968 | Common:1; Rare:30 | ||||
| chr19:40285186-40285235 | Rare:11 | ||||
| chr19:40285243-40285528 | Common:1; Rare:107 | ||||
| chr19:40348388-40348739 | Common:4; Rare:117 |