| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:58476828-58476933 | Rare:34 | ||||
| chr19:58499175-58499733 | Common:3; Rare:195; Clinvar:9; Clinvar (benign):2 | ||||
| chr19:58519097-58519197 | Rare:23 | ||||
| chr19:58519333-58519416 | Common:1; Rare:17 | ||||
| chr19:58519487-58520073 | Rare:147 | ||||
| chr19:58538292-58538954 | Common:1; Rare:214 | ||||
| chr19:58543710-58543771 | Common:1; Rare:14 | ||||
| chr19:58543941-58544034 | Rare:21 | ||||
| chr19:58544037-58544207 | Common:2; Rare:59 | ||||
| chr19:58544296-58544556 | Rare:122 | ||||
| chr19:58544611-58544824 | Rare:90 | ||||
| chr19:58554913-58555461 | Common:3; Rare:172 | ||||
| chr19:58558474-58558768 | Rare:95 | ||||
| chr19:58558839-58559222 | Common:2; Rare:118 | ||||
| chr19:58559375-58559788 | Common:3; Rare:81 |