| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:47256472-47256585 | Rare:42 | ||||
| chr19:47309719-47309874 | Common:1; Rare:28 | ||||
| chr19:47349088-47349387 | Rare:85 | ||||
| chr19:47484182-47484395 | Common:2; Rare:67 | ||||
| chr19:47780664-47780917 | Common:5; Rare:95 | ||||
| chr19:47781106-47781409 | Rare:118 | ||||
| chr19:48170294-48170704 | Common:2; Rare:108 | ||||
| chr19:48321230-48321485 | Common:2; Rare:73 | ||||
| chr19:48445909-48446012 | Rare:39 | ||||
| chr19:48469095-48469431 | Common:3; Rare:93 | ||||
| chr19:48619139-48619560 | Common:1; Rare:138 | ||||
| chr19:48624139-48624410 | Common:1; Rare:73 | ||||
| chr19:48811003-48811119 | Rare:40 | ||||
| chr19:48965357-48965609 | Rare:80; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):3 | ||||
| chr19:48993253-48993533 | Common:3; Rare:124; Clinvar:3; Clinvar (benign):2 |