Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:27890406-27890825 | Rare:107 | ||||
chr2:28392633-28392858 | Rare:81 | ||||
chr2:28751728-28752146 | Common:1; Rare:169 | ||||
chr2:28870262-28870437 | Rare:66 | ||||
chr2:30447136-30447283 | Common:3; Rare:50 | ||||
chr2:32039738-32039842 | Rare:34 | ||||
chr2:32165711-32165898 | Common:1; Rare:72 | ||||
chr2:33599222-33599549 | Common:1; Rare:117 | ||||
chr2:37084312-37084559 | Common:3; Rare:92 | ||||
chr2:37231553-37231696 | Common:4; Rare:80; Clinvar (benign):3 | ||||
chr2:37324761-37324950 | Common:1; Rare:79 | ||||
chr2:37344572-37344726 | Common:1; Rare:60 | ||||
chr2:38076138-38076291 | Rare:38 | ||||
chr2:38751348-38751625 | Common:4; Rare:126 | ||||
chr2:38875897-38876047 | Common:1; Rare:52 |