Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:28751707-28752134 | Common:2; Rare:176 | ||||
chr2:28870267-28870429 | Rare:60 | ||||
chr2:30146639-30147034 | Common:5; Rare:127 | ||||
chr2:32039753-32039851 | Rare:29 | ||||
chr2:32165745-32165893 | Common:1; Rare:51 | ||||
chr2:32628031-32628131 | Rare:31 | ||||
chr2:33599283-33599445 | Common:1; Rare:47 | ||||
chr2:37084276-37084544 | Common:3; Rare:96 | ||||
chr2:37231563-37231696 | Common:4; Rare:72; Clinvar (benign):3 | ||||
chr2:37324698-37324950 | Common:1; Rare:100 | ||||
chr2:38751349-38751616 | Common:3; Rare:121 | ||||
chr2:38875902-38876064 | Common:1; Rare:56 | ||||
chr2:39437307-39437453 | Common:2; Rare:50 | ||||
chr2:40511759-40512003 | Common:1; Rare:45 | ||||
chr2:43595940-43596194 | Common:1; Rare:87 |