Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:42958849-42959078 | Common:2; Rare:61; Clinvar:5; Clinvar (benign):2 | ||||
chr1:43172228-43172335 | Common:1; Rare:57 | ||||
chr1:43358703-43359102 | Common:7; Rare:121 | ||||
chr1:43367961-43368149 | Rare:48 | ||||
chr1:43389765-43389945 | Common:3; Rare:76 | ||||
chr1:43974778-43975068 | Common:3; Rare:77 | ||||
chr1:44775453-44775599 | Rare:56 | ||||
chr1:44775848-44776124 | Common:2; Rare:102 | ||||
chr1:44986545-44986733 | Common:2; Rare:33; Clinvar (benign):1 | ||||
chr1:45326766-45326921 | Rare:38 | ||||
chr1:45339962-45340178 | Rare:68 | ||||
chr1:45340388-45340566 | Common:1; Rare:44; Clinvar:1 | ||||
chr1:45500005-45500359 | Common:2; Rare:83; Clinvar:4; Clinvar (pathogenic):3 | ||||
chr1:45521809-45522072 | Common:1; Rare:101 | ||||
chr1:45522790-45522895 | Rare:16 |