| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:39344569-39344670 | Rare:21 | ||||
| chr19:39405263-39405355 | Common:1; Rare:17 | ||||
| chr19:39470246-39470459 | Common:1; Rare:48 | ||||
| chr19:39539189-39539424 | Common:1; Rare:49 | ||||
| chr19:39943725-39943833 | Rare:18 | ||||
| chr19:39972144-39972553 | Common:1; Rare:102 | ||||
| chr19:39974384-39974820 | Common:7; Rare:114 | ||||
| chr19:39981994-39982042 | Common:3; Rare:5 | ||||
| chr19:40607222-40607529 | Common:1; Rare:76; Clinvar:1; Clinvar (benign):2 | ||||
| chr19:40765349-40765528 | Common:1; Rare:32 | ||||
| chr19:40783153-40783375 | Common:3; Rare:48 | ||||
| chr19:41248540-41248821 | Common:1; Rare:78 | ||||
| chr19:41294337-41294603 | Rare:57 | ||||
| chr19:41294636-41294811 | Rare:33 | ||||
| chr19:41322443-41322720 | Common:1; Rare:83 |