Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:42958816-42959020 | Common:2; Rare:50; Clinvar:3; Clinvar (benign):3 | ||||
chr1:43171889-43172181 | Common:1; Rare:96 | ||||
chr1:43271350-43271668 | Common:5; Rare:50 | ||||
chr1:43285528-43285706 | Common:2; Rare:31 | ||||
chr1:43358662-43359006 | Common:7; Rare:110 | ||||
chr1:43367927-43368208 | Rare:72 | ||||
chr1:43386952-43387133 | Rare:31 | ||||
chr1:43387509-43387775 | Rare:54 | ||||
chr1:43389757-43389986 | Common:4; Rare:99; Clinvar:1 | ||||
chr1:43649869-43650210 | Rare:80 | ||||
chr1:43946574-43947000 | Rare:115 | ||||
chr1:43957262-43957460 | Rare:60 | ||||
chr1:43974896-43975038 | Common:3; Rare:42 | ||||
chr1:43991378-43991657 | Common:2; Rare:108 | ||||
chr1:44031343-44031668 | Common:2; Rare:66 |