Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:11805628-11805741 | Rare:25 | ||||
chr1:11805775-11806268 | Common:2; Rare:133; Clinvar:2 | ||||
chr1:11806338-11806497 | Common:2; Rare:38 | ||||
chr1:11806687-11806769 | Common:1; Rare:27 | ||||
chr1:11858893-11859201 | Rare:79 | ||||
chr1:11926354-11926648 | Common:6; Rare:79 | ||||
chr1:11934454-11934836 | Common:6; Rare:113; Clinvar:7; Clinvar (benign):1 | ||||
chr1:11979857-11980238 | Common:1; Rare:79 | ||||
chr1:11980304-11980516 | Common:3; Rare:67; Clinvar:1; Clinvar (benign):6 | ||||
chr1:11980851-11980899 | Rare:15 | ||||
chr1:12019185-12019581 | Common:5; Rare:142 | ||||
chr1:12019691-12019913 | Rare:51 | ||||
chr1:12166892-12167048 | Common:1; Rare:45 | ||||
chr1:12229922-12230135 | Common:2; Rare:69 | ||||
chr1:12615944-12616341 | Common:2; Rare:77 |