Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:42456436-42456586 | Rare:63 | ||||
chr1:42766993-42767309 | Common:4; Rare:106; Clinvar (benign):1 | ||||
chr1:42816972-42817165 | Common:1; Rare:59 | ||||
chr1:42817194-42817483 | Rare:99 | ||||
chr1:42846401-42846638 | Common:1; Rare:65 | ||||
chr1:42958709-42959078 | Common:4; Rare:95; Clinvar:6; Clinvar (benign):4 | ||||
chr1:42959177-42959496 | Common:2; Rare:73 | ||||
chr1:43172217-43172335 | Common:1; Rare:59 | ||||
chr1:43358660-43359047 | Common:7; Rare:128 | ||||
chr1:43367990-43368216 | Rare:60 | ||||
chr1:43389747-43389945 | Common:3; Rare:89 | ||||
chr1:43707352-43707589 | Common:2; Rare:68 | ||||
chr1:43946653-43946967 | Rare:84 | ||||
chr1:43974817-43975019 | Common:3; Rare:57 | ||||
chr1:43979094-43979250 | Common:2; Rare:58 |