| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:39390850-39391425 | Common:1; Rare:215 | ||||
| chr19:39406689-39406870 | Rare:65 | ||||
| chr19:39435882-39436154 | Common:4; Rare:103 | ||||
| chr19:39480710-39480912 | Common:3; Rare:110; Clinvar (pathogenic):1 | ||||
| chr19:39834143-39834377 | Common:2; Rare:66 | ||||
| chr19:39846335-39846487 | Common:1; Rare:70 | ||||
| chr19:39970900-39971202 | Common:4; Rare:89 | ||||
| chr19:39996956-39997101 | Common:4; Rare:50 | ||||
| chr19:40056135-40056260 | Rare:16 | ||||
| chr19:40090873-40090968 | Common:1; Rare:26 | ||||
| chr19:40285233-40285622 | Common:3; Rare:133 | ||||
| chr19:40348347-40348746 | Common:4; Rare:129 | ||||
| chr19:40444298-40444513 | Common:3; Rare:61 | ||||
| chr19:40465735-40466101 | Common:3; Rare:106 | ||||
| chr19:40716880-40717009 | Common:1; Rare:42 |