Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:32627945-32628139 | Rare:63 | ||||
chr2:33476547-33476691 | Common:2; Rare:24 | ||||
chr2:33599222-33599434 | Common:1; Rare:80 | ||||
chr2:37084293-37084550 | Common:3; Rare:96 | ||||
chr2:37231542-37231726 | Common:4; Rare:108; Clinvar (benign):4 | ||||
chr2:37324698-37324915 | Common:1; Rare:82 | ||||
chr2:37671514-37671745 | Common:1; Rare:93 | ||||
chr2:38076143-38076278 | Rare:34 | ||||
chr2:38875902-38876075 | Common:1; Rare:61 | ||||
chr2:39120995-39121125 | Rare:44 | ||||
chr2:39437065-39437456 | Common:4; Rare:141 | ||||
chr2:40511764-40511922 | Common:1; Rare:32 | ||||
chr2:40512337-40512773 | Common:3; Rare:84 | ||||
chr2:42169168-42169436 | Common:1; Rare:132 | ||||
chr2:42792537-42792868 | Common:3; Rare:96 |