| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:37210510-37210736 | Common:2; Rare:54 | ||||
| chr19:37218140-37218260 | Rare:18 | ||||
| chr19:37317666-37317911 | Common:6; Rare:59 | ||||
| chr19:37370929-37371212 | Common:5; Rare:58 | ||||
| chr19:37467186-37467546 | Common:2; Rare:101 | ||||
| chr19:37779568-37779667 | Rare:21 | ||||
| chr19:37907021-37907293 | Common:1; Rare:62 | ||||
| chr19:38315917-38316256 | Common:1; Rare:88 | ||||
| chr19:38374411-38374849 | Rare:171 | ||||
| chr19:38389712-38389833 | Rare:14 | ||||
| chr19:38618932-38619325 | Common:3; Rare:110 | ||||
| chr19:38647372-38647748 | Common:3; Rare:132 | ||||
| chr19:38852319-38852548 | Rare:53 | ||||
| chr19:38899572-38900026 | Rare:133 | ||||
| chr19:38930720-38931013 | Common:3; Rare:85; Clinvar:2; Clinvar (benign):3 |