Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:42846392-42846638 | Common:1; Rare:68 | ||||
chr1:42958830-42959078 | Common:4; Rare:70; Clinvar:6; Clinvar (benign):4 | ||||
chr1:43172228-43172343 | Common:1; Rare:61 | ||||
chr1:43358674-43359090 | Common:7; Rare:128 | ||||
chr1:43367961-43368183 | Rare:58 | ||||
chr1:43389763-43389950 | Common:3; Rare:81 | ||||
chr1:43974808-43975026 | Common:3; Rare:60 | ||||
chr1:44674421-44674731 | Common:3; Rare:79 | ||||
chr1:44739598-44739942 | Common:3; Rare:137 | ||||
chr1:44775452-44775599 | Rare:57 | ||||
chr1:44775848-44776074 | Common:2; Rare:91 | ||||
chr1:45339996-45340227 | Rare:83; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr1:45521859-45522013 | Common:1; Rare:62 | ||||
chr1:45550721-45551071 | Common:3; Rare:87 | ||||
chr1:45583931-45584060 | Rare:47 |