Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:4995756-4995987 | Common:2; Rare:67; Clinvar (pathogenic):1 | ||||
chr10:10798193-10798448 | Common:2; Rare:47 | ||||
chr10:15546201-15546307 | Rare:25 | ||||
chr10:15599771-15599839 | Rare:16 | ||||
chr10:15606283-15606586 | Rare:88 | ||||
chr10:15718517-15718659 | Common:1; Rare:34 | ||||
chr10:15718920-15719015 | Rare:20 | ||||
chr10:15719043-15719239 | Common:3; Rare:39 | ||||
chr10:17023420-17023638 | Rare:49 | ||||
chr10:22251854-22252099 | Rare:53 | ||||
chr10:29462268-29462592 | Common:2; Rare:72 | ||||
chr10:29463540-29463793 | Common:2; Rare:58; Clinvar:1 | ||||
chr10:29464637-29464886 | Common:5; Rare:36 | ||||
chr10:29465154-29465250 | Rare:26 | ||||
chr10:29467820-29468034 | Rare:47 |