| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:38930677-38931059 | Common:3; Rare:116; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr19:39125524-39125886 | Common:2; Rare:93 | ||||
| chr19:39335657-39335835 | Common:2; Rare:37 | ||||
| chr19:39335971-39336207 | Common:1; Rare:62 | ||||
| chr19:39341861-39342049 | Common:1; Rare:45 | ||||
| chr19:39390807-39390934 | Rare:51; Clinvar:1 | ||||
| chr19:39390954-39391503 | Common:1; Rare:209 | ||||
| chr19:39391638-39391709 | Rare:23 | ||||
| chr19:39406673-39407350 | Rare:190 | ||||
| chr19:39407616-39407764 | Rare:35 | ||||
| chr19:39412222-39412285 | Rare:35 | ||||
| chr19:39412544-39412974 | Common:3; Rare:118 | ||||
| chr19:39413374-39413805 | Common:3; Rare:107 | ||||
| chr19:39435873-39436346 | Common:8; Rare:171 | ||||
| chr19:39445298-39445761 | Common:5; Rare:142 |