Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:27663345-27663917 | Rare:179 | ||||
chr2:27890348-27890812 | Common:1; Rare:128 | ||||
chr2:28751706-28752011 | Common:2; Rare:135 | ||||
chr2:28894352-28894695 | Common:5; Rare:111 | ||||
chr2:31233997-31234164 | Rare:43 | ||||
chr2:32039753-32039878 | Rare:38 | ||||
chr2:32627948-32628123 | Rare:56 | ||||
chr2:37084300-37084561 | Common:3; Rare:100 | ||||
chr2:37231417-37231733 | Common:5; Rare:160; Clinvar:1; Clinvar (benign):4 | ||||
chr2:37324689-37324887 | Rare:82 | ||||
chr2:37344537-37344741 | Common:2; Rare:73 | ||||
chr2:37925072-37925364 | Common:2; Rare:99 | ||||
chr2:38075931-38076291 | Common:2; Rare:90 | ||||
chr2:38875906-38876040 | Common:1; Rare:41 | ||||
chr2:39437104-39437480 | Common:4; Rare:133 |