Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:27663385-27663434 | Rare:13 | ||||
chr2:27663607-27663911 | Rare:108 | ||||
chr2:27771607-27771979 | Common:1; Rare:118 | ||||
chr2:28751608-28752136 | Common:3; Rare:217 | ||||
chr2:28870262-28870475 | Rare:86 | ||||
chr2:30447131-30447303 | Common:3; Rare:58 | ||||
chr2:32039761-32039860 | Rare:29 | ||||
chr2:32063362-32063673 | Common:1; Rare:115; Clinvar:1 | ||||
chr2:32165680-32165898 | Common:1; Rare:86 | ||||
chr2:37084321-37084561 | Common:3; Rare:92 | ||||
chr2:37231559-37231701 | Common:4; Rare:78; Clinvar (benign):3 | ||||
chr2:37324738-37324909 | Common:1; Rare:71 | ||||
chr2:37671625-37671787 | Common:3; Rare:70 | ||||
chr2:38076149-38076309 | Common:1; Rare:40 | ||||
chr2:38875891-38875999 | Common:1; Rare:31 |