Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:11691601-11691755 | Common:2; Rare:29 | ||||
chr1:11735963-11736160 | Common:2; Rare:50 | ||||
chr1:11736544-11736572 | Rare:6 | ||||
chr1:11803574-11803804 | Rare:39 | ||||
chr1:11805668-11805739 | Rare:18 | ||||
chr1:11805852-11806295 | Common:2; Rare:126; Clinvar:2 | ||||
chr1:11806699-11806746 | Common:1; Rare:15 | ||||
chr1:11926354-11926623 | Common:6; Rare:75 | ||||
chr1:11934475-11934769 | Common:5; Rare:94; Clinvar:5; Clinvar (benign):1 | ||||
chr1:11934912-11934956 | Rare:6 | ||||
chr1:11979897-11980369 | Common:4; Rare:121; Clinvar:1; Clinvar (benign):2 | ||||
chr1:11980370-11980495 | Common:2; Rare:40; Clinvar (benign):3 | ||||
chr1:12019180-12019656 | Common:5; Rare:169 | ||||
chr1:12229902-12230114 | Common:2; Rare:66 | ||||
chr1:12617926-12618177 | Common:1; Rare:55 |