| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:46601649-46602283 | Common:2; Rare:190 | ||||
| chr19:46625030-46625594 | Common:4; Rare:213 | ||||
| chr19:46634170-46634540 | Common:3; Rare:68 | ||||
| chr19:46661060-46661570 | Rare:434 | ||||
| chr19:46661603-46661787 | Common:1; Rare:41 | ||||
| chr19:46697051-46698015 | Common:19; Rare:623 | ||||
| chr19:46713632-46714032 | Common:5; Rare:235 | ||||
| chr19:46714035-46714610 | Common:7; Rare:254 | ||||
| chr19:46716130-46716530 | Common:2; Rare:145 | ||||
| chr19:46716964-46717364 | Common:11; Rare:329 | ||||
| chr19:46717453-46718252 | Common:6; Rare:226 | ||||
| chr19:46730860-46731310 | Rare:147 | ||||
| chr19:46736512-46736912 | Common:7; Rare:140 | ||||
| chr19:46745708-46746108 | Common:18; Rare:322; Clinvar (benign):4 | ||||
| chr19:46746190-46746801 | Common:19; Rare:535 |