Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:36573195-36573388 | Common:3; Rare:59 | ||||
chr19:36666809-36666946 | Rare:38 | ||||
chr19:36687370-36687634 | Common:3; Rare:83 | ||||
chr19:36850262-36850396 | Rare:20 | ||||
chr19:36850770-36850882 | Rare:24 | ||||
chr19:37078320-37078487 | Common:3; Rare:40 | ||||
chr19:37218140-37218254 | Rare:17 | ||||
chr19:37317635-37317919 | Common:6; Rare:76 | ||||
chr19:37467190-37467529 | Common:2; Rare:97 | ||||
chr19:37594739-37594886 | Rare:42 | ||||
chr19:37779579-37779662 | Rare:18 | ||||
chr19:38433529-38433714 | Common:1; Rare:36 | ||||
chr19:38528306-38528692 | Common:2; Rare:128; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
chr19:38831753-38832061 | Common:4; Rare:93; Clinvar (benign):1 | ||||
chr19:38899513-38900039 | Rare:159 |