Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:27628981-27629077 | Common:1; Rare:49 | ||||
chr2:27663379-27663468 | Rare:23 | ||||
chr2:27663603-27663917 | Rare:112 | ||||
chr2:27771652-27772029 | Common:1; Rare:116 | ||||
chr2:27890402-27890815 | Rare:105 | ||||
chr2:28751507-28752134 | Common:4; Rare:249 | ||||
chr2:28870267-28870418 | Rare:56 | ||||
chr2:32039747-32039851 | Rare:34 | ||||
chr2:32165737-32165901 | Common:1; Rare:63 | ||||
chr2:32627906-32628119 | Rare:59 | ||||
chr2:37084319-37084561 | Common:3; Rare:93 | ||||
chr2:37156933-37157115 | Common:1; Rare:60 | ||||
chr2:37231559-37231714 | Common:4; Rare:86; Clinvar (benign):3 | ||||
chr2:37324700-37324964 | Common:1; Rare:105 | ||||
chr2:38076138-38076291 | Rare:38 |