| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:37370951-37371216 | Common:5; Rare:54 | ||||
| chr19:37467190-37467519 | Common:2; Rare:95 | ||||
| chr19:37469268-37469405 | Common:2; Rare:39 | ||||
| chr19:37594740-37594886 | Rare:42 | ||||
| chr19:37655449-37655491 | Common:1; Rare:15 | ||||
| chr19:37779579-37779662 | Rare:18 | ||||
| chr19:38264345-38264677 | Common:5; Rare:83 | ||||
| chr19:38315898-38316256 | Common:1; Rare:98 | ||||
| chr19:38374413-38374812 | Rare:148 | ||||
| chr19:38618890-38619307 | Common:4; Rare:121 | ||||
| chr19:38708000-38708188 | Rare:33 | ||||
| chr19:38736971-38737124 | Common:2; Rare:20 | ||||
| chr19:38812928-38813222 | Common:1; Rare:56 | ||||
| chr19:38815576-38815971 | Common:2; Rare:145; Clinvar (benign):1 | ||||
| chr19:38816286-38816525 | Common:2; Rare:90; Clinvar (benign):1 |