Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:55230427-55230640 | Common:3; Rare:99 | ||||
chr19:56301820-56302066 | Common:3; Rare:44 | ||||
chr2:1608036-1608288 | Common:1; Rare:47 | ||||
chr2:1625408-1625668 | Common:1; Rare:54 | ||||
chr2:1707822-1707944 | Common:3; Rare:23 | ||||
chr2:12715909-12716060 | Common:2; Rare:34 | ||||
chr2:20447729-20447823 | Rare:24 | ||||
chr2:20447833-20448008 | Rare:56 | ||||
chr2:20448362-20448844 | Common:2; Rare:119 | ||||
chr2:26191514-26191786 | Common:2; Rare:75; Clinvar:3 | ||||
chr2:36548291-36548865 | Common:1; Rare:191 | ||||
chr2:37671455-37671578 | Rare:24 | ||||
chr2:38482282-38482493 | Common:2; Rare:54 | ||||
chr2:55870998-55871223 | Common:1; Rare:52; Clinvar (benign):1 | ||||
chr2:56185749-56185992 | Common:2; Rare:66 |