| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:36850770-36850921 | Rare:38 | ||||
| chr19:36916009-36916358 | Common:3; Rare:58 | ||||
| chr19:37078188-37078483 | Common:4; Rare:69 | ||||
| chr19:37218129-37218245 | Rare:21 | ||||
| chr19:37317664-37317920 | Common:6; Rare:60 | ||||
| chr19:37370973-37371226 | Common:3; Rare:51 | ||||
| chr19:37467190-37467525 | Common:2; Rare:97 | ||||
| chr19:37469203-37469405 | Common:2; Rare:60 | ||||
| chr19:37594732-37594917 | Rare:52 | ||||
| chr19:37779572-37779662 | Rare:20 | ||||
| chr19:37907045-37907293 | Rare:54 | ||||
| chr19:38336317-38336466 | Common:1; Rare:31 | ||||
| chr19:38618958-38619256 | Common:3; Rare:85 | ||||
| chr19:38831768-38832064 | Common:4; Rare:84; Clinvar (benign):1 | ||||
| chr19:38852311-38852635 | Rare:79 |