| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:37469173-37469390 | Common:2; Rare:65 | ||||
| chr19:37551270-37551395 | Rare:42 | ||||
| chr19:37594732-37594886 | Rare:43 | ||||
| chr19:37655422-37655570 | Common:2; Rare:61 | ||||
| chr19:37779579-37779653 | Rare:18 | ||||
| chr19:37907045-37907284 | Rare:52 | ||||
| chr19:38224150-38224322 | Rare:42 | ||||
| chr19:38315740-38316119 | Rare:123 | ||||
| chr19:38374413-38374836 | Rare:164 | ||||
| chr19:38618947-38619307 | Common:3; Rare:101 | ||||
| chr19:38647372-38647748 | Common:3; Rare:132 | ||||
| chr19:38831753-38832064 | Common:4; Rare:94; Clinvar (benign):1 | ||||
| chr19:38852319-38852582 | Rare:65 | ||||
| chr19:38899546-38900069 | Rare:159 | ||||
| chr19:38930723-38931002 | Common:3; Rare:80; Clinvar:2; Clinvar (benign):3 |