Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:30231668-30231757 | Rare:26 | ||||
chr2:30447069-30447299 | Common:4; Rare:81 | ||||
chr2:32039738-32039842 | Rare:34 | ||||
chr2:32165732-32165898 | Common:1; Rare:63 | ||||
chr2:32628037-32628139 | Rare:33 | ||||
chr2:33599224-33599555 | Common:1; Rare:117 | ||||
chr2:36597979-36598284 | Common:19; Rare:140 | ||||
chr2:37084319-37084561 | Common:3; Rare:93 | ||||
chr2:37231551-37231703 | Common:4; Rare:86; Clinvar (benign):3 | ||||
chr2:38076145-38076291 | Rare:38 | ||||
chr2:38751332-38751579 | Common:3; Rare:112 | ||||
chr2:38875892-38876105 | Common:1; Rare:75 | ||||
chr2:39437104-39437447 | Common:4; Rare:119 | ||||
chr2:43595982-43596191 | Common:1; Rare:66 | ||||
chr2:44361758-44361958 | Common:1; Rare:61 |