Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:20448348-20448839 | Common:3; Rare:124 | ||||
chr2:20450905-20451069 | Rare:41 | ||||
chr2:23617373-23617753 | Rare:73 | ||||
chr2:23617989-23618003 | Rare:4 | ||||
chr2:26193585-26194052 | Common:2; Rare:125; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):3 | ||||
chr2:27735605-27735812 | Rare:47 | ||||
chr2:28391114-28391305 | Rare:43 | ||||
chr2:28391691-28391937 | Common:3; Rare:48 | ||||
chr2:28394657-28394791 | Common:1; Rare:32 | ||||
chr2:28396512-28396814 | Common:1; Rare:50 | ||||
chr2:28607042-28607295 | Common:1; Rare:69 | ||||
chr2:28625367-28625640 | Rare:50 | ||||
chr2:28664515-28664579 | Common:2; Rare:13 | ||||
chr2:38515473-38515620 | Common:1; Rare:30 | ||||
chr2:42811123-42811181 | Rare:17 |