Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:11663945-11664205 | Common:2; Rare:60 | ||||
chr1:11664724-11664802 | Rare:10 | ||||
chr1:11680572-11680734 | Common:1; Rare:51 | ||||
chr1:11736020-11736206 | Common:3; Rare:57 | ||||
chr1:11762141-11762263 | Rare:64 | ||||
chr1:11805867-11806278 | Common:2; Rare:113; Clinvar:2 | ||||
chr1:11829524-11829902 | Common:5; Rare:64 | ||||
chr1:11980161-11980499 | Common:5; Rare:111; Clinvar:1; Clinvar (benign):5 | ||||
chr1:12019263-12019580 | Common:5; Rare:112 | ||||
chr1:12229944-12230115 | Common:1; Rare:55 | ||||
chr1:12618174-12618475 | Common:3; Rare:65 | ||||
chr1:12746085-12746302 | Common:4; Rare:33 | ||||
chr1:13700170-13700277 | Rare:44 | ||||
chr1:13749154-13749455 | Common:2; Rare:107 | ||||
chr1:15247086-15247327 | Common:7; Rare:87 |