| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:36916013-36916371 | Common:3; Rare:63 | ||||
| chr19:37078181-37078483 | Common:4; Rare:70 | ||||
| chr19:37218124-37218274 | Rare:32 | ||||
| chr19:37317659-37317920 | Common:6; Rare:62 | ||||
| chr19:37370951-37371222 | Common:5; Rare:57 | ||||
| chr19:37467190-37467519 | Common:2; Rare:95 | ||||
| chr19:37506891-37506948 | Rare:14 | ||||
| chr19:37594739-37594932 | Rare:56 | ||||
| chr19:37779579-37779662 | Rare:18 | ||||
| chr19:37907063-37907293 | Rare:52 | ||||
| chr19:38315926-38316256 | Common:1; Rare:81 | ||||
| chr19:38374405-38374835 | Rare:165 | ||||
| chr19:38831756-38832052 | Common:4; Rare:90; Clinvar (benign):1 | ||||
| chr19:38852324-38852383 | Rare:15 | ||||
| chr19:38899528-38900018 | Rare:149 |