Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:27583010-27583101 | Rare:35 | ||||
chr2:27628981-27629058 | Common:1; Rare:39 | ||||
chr2:27663537-27663917 | Rare:135 | ||||
chr2:27771652-27771766 | Common:1; Rare:43 | ||||
chr2:28751489-28752044 | Common:4; Rare:224 | ||||
chr2:28870267-28870463 | Rare:75 | ||||
chr2:30447174-30447328 | Common:1; Rare:49 | ||||
chr2:31233968-31234158 | Rare:52 | ||||
chr2:32011006-32011153 | Rare:46 | ||||
chr2:32039753-32039893 | Rare:43 | ||||
chr2:32165745-32165898 | Common:1; Rare:57 | ||||
chr2:33599210-33599445 | Common:1; Rare:89 | ||||
chr2:37084304-37084561 | Common:3; Rare:98 | ||||
chr2:37196394-37196508 | Rare:37 | ||||
chr2:37231559-37231703 | Common:4; Rare:79; Clinvar (benign):3 |