Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:32246958-32247236 | Rare:46 | ||||
chr1:32291824-32292156 | Common:1; Rare:95 | ||||
chr1:32394403-32394680 | Common:1; Rare:78 | ||||
chr1:32650489-32650638 | Common:1; Rare:72 | ||||
chr1:32650907-32651318 | Common:2; Rare:151 | ||||
chr1:32780261-32780564 | Common:1; Rare:61; Clinvar:1; Clinvar (benign):2 | ||||
chr1:32806383-32806491 | Rare:23; Clinvar (benign):1 | ||||
chr1:32817233-32817674 | Rare:116; Clinvar:5 | ||||
chr1:32901245-32901564 | Common:1; Rare:79 | ||||
chr1:33021445-33021704 | Rare:64; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr1:33080992-33081158 | Common:2; Rare:38 | ||||
chr1:33430994-33431252 | Common:2; Rare:69 | ||||
chr1:34985276-34985419 | Common:2; Rare:52 | ||||
chr1:35079330-35079422 | Common:3; Rare:27 | ||||
chr1:35193034-35193403 | Common:1; Rare:128 |