Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:54887158-54887418 | Common:3; Rare:85; Clinvar:2; Clinvar (benign):1 | ||||
chr1:56645264-56645381 | Common:1; Rare:50 | ||||
chr1:58546706-58546845 | Common:4; Rare:69 | ||||
chr1:58783991-58784227 | Rare:57 | ||||
chr1:59814903-59815039 | Rare:43 | ||||
chr1:61076996-61077400 | Common:3; Rare:97 | ||||
chr1:61082149-61082467 | Rare:116 | ||||
chr1:61725028-61725208 | Rare:88 | ||||
chr1:61742361-61742553 | Rare:57 | ||||
chr1:62436250-62436301 | Common:1; Rare:12 | ||||
chr1:62436800-62437130 | Common:1; Rare:88 | ||||
chr1:62688266-62688504 | Common:1; Rare:99 | ||||
chr1:62784069-62784180 | Rare:44 | ||||
chr1:63367522-63367668 | Rare:43 | ||||
chr1:63523176-63523596 | Common:3; Rare:107 |