Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:35545397-35545689 | Common:4; Rare:90 | ||||
chr19:35628880-35629085 | Common:3; Rare:62 | ||||
chr19:35648110-35648391 | Common:1; Rare:64; Clinvar:1; Clinvar (benign):1 | ||||
chr19:35745397-35745661 | Rare:84 | ||||
chr19:35900538-35900623 | Rare:16 | ||||
chr19:36014214-36014529 | Common:2; Rare:86 | ||||
chr19:36114852-36114959 | Common:1; Rare:51 | ||||
chr19:36215058-36215177 | Rare:37 | ||||
chr19:36489549-36489633 | Rare:15 | ||||
chr19:36528244-36528416 | Common:1; Rare:40 | ||||
chr19:36605263-36605319 | Rare:14 | ||||
chr19:36916009-36916347 | Common:3; Rare:55 | ||||
chr19:37078158-37078449 | Common:2; Rare:70 | ||||
chr19:37469273-37469353 | Common:2; Rare:21 | ||||
chr19:38618923-38619246 | Common:3; Rare:98 |