Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:36573276-36573384 | Common:3; Rare:20 | ||||
chr19:36850227-36850391 | Rare:34 | ||||
chr19:36850783-36850906 | Rare:29 | ||||
chr19:36916006-36916427 | Common:3; Rare:76 | ||||
chr19:37317666-37317920 | Common:6; Rare:60 | ||||
chr19:38618932-38619246 | Common:3; Rare:95 | ||||
chr19:38831761-38832061 | Common:4; Rare:90; Clinvar (benign):1 | ||||
chr19:38852319-38852605 | Rare:69 | ||||
chr19:38899514-38900018 | Rare:153 | ||||
chr19:38930726-38930996 | Common:3; Rare:78; Clinvar:2; Clinvar (benign):3 | ||||
chr19:39342356-39342505 | Common:2; Rare:44 | ||||
chr19:39391074-39391420 | Common:1; Rare:143 | ||||
chr19:39435848-39436155 | Common:6; Rare:111 | ||||
chr19:39834124-39834478 | Common:3; Rare:93 | ||||
chr19:40348510-40348763 | Common:3; Rare:80 |