Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:21569235-21569415 | Common:7; Rare:51 | ||||
chr19:23274201-23274391 | Common:1; Rare:45 | ||||
chr19:23762848-23763011 | Common:2; Rare:53 | ||||
chr19:27793228-27793477 | Common:4; Rare:57 | ||||
chr19:27793891-27794061 | Common:1; Rare:36 | ||||
chr19:30426671-30426831 | Common:1; Rare:30 | ||||
chr19:42010445-42010583 | Common:1; Rare:21 | ||||
chr19:42129638-42129893 | Rare:44 | ||||
chr19:42396922-42397174 | Common:1; Rare:58 | ||||
chr19:46860842-46861111 | Common:3; Rare:87 | ||||
chr19:48259768-48259876 | Rare:27 | ||||
chr19:48966271-48966703 | Rare:146; Clinvar:2; Clinvar (pathogenic):2 | ||||
chr19:50419653-50419844 | Common:1; Rare:48 | ||||
chr19:51333902-51334128 | Common:5; Rare:54 | ||||
chr19:51394265-51394535 | Common:4; Rare:55 |