Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:114511222-114511349 | Common:3; Rare:48 | ||||
chr1:115089462-115089578 | Common:1; Rare:48 | ||||
chr1:116667672-116667853 | Common:1; Rare:66 | ||||
chr1:116754351-116754470 | Rare:34 | ||||
chr1:117060171-117060349 | Common:2; Rare:42 | ||||
chr1:117367314-117367490 | Common:4; Rare:64 | ||||
chr1:117605805-117606052 | Rare:73 | ||||
chr1:117929568-117929821 | Common:4; Rare:78 | ||||
chr1:119140594-119140782 | Common:1; Rare:68; Clinvar (pathogenic):1 | ||||
chr1:119648138-119648350 | Common:3; Rare:77 | ||||
chr1:121184907-121185081 | Rare:60 | ||||
chr1:145214943-145215004 | Rare:10 | ||||
chr1:145823922-145824296 | Rare:129 | ||||
chr1:145858996-145859175 | Rare:51 | ||||
chr1:145918680-145919013 | Common:2; Rare:74 |