Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:20654365-20654633 | Common:3; Rare:76; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr1:20655514-20655618 | Rare:33; Clinvar (benign):1 | ||||
chr1:21857015-21857324 | Common:1; Rare:95; Clinvar:5; Clinvar (benign):2 | ||||
chr1:21887247-21887609 | Common:2; Rare:146; Clinvar:10; Clinvar (benign):2 | ||||
chr1:22086438-22086863 | Common:2; Rare:72 | ||||
chr1:23397546-23397926 | Common:1; Rare:118 | ||||
chr1:24129416-24129640 | Rare:57 | ||||
chr1:24331120-24331388 | Common:1; Rare:48 | ||||
chr1:24333849-24334142 | Common:2; Rare:40 | ||||
chr1:24334364-24334928 | Common:1; Rare:107 | ||||
chr1:26862073-26862338 | Rare:37 | ||||
chr1:26863969-26864283 | Rare:56 | ||||
chr1:26864442-26864721 | Common:1; Rare:57 | ||||
chr1:26865060-26865125 | Common:1; Rare:25 | ||||
chr1:27353453-27353724 | Common:2; Rare:64 |