Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:28751687-28752134 | Common:2; Rare:191 | ||||
chr2:28870260-28870475 | Rare:88 | ||||
chr2:30146915-30147016 | Common:2; Rare:26 | ||||
chr2:32039761-32039854 | Rare:28 | ||||
chr2:32165705-32165886 | Common:1; Rare:63 | ||||
chr2:32627945-32628122 | Rare:56 | ||||
chr2:33476544-33476646 | Common:2; Rare:16 | ||||
chr2:33599217-33599434 | Common:1; Rare:84 | ||||
chr2:37084276-37084561 | Common:3; Rare:107 | ||||
chr2:37231457-37231706 | Common:5; Rare:128; Clinvar (benign):3 | ||||
chr2:37324698-37324950 | Common:1; Rare:100 | ||||
chr2:37671514-37671745 | Common:1; Rare:93 | ||||
chr2:37925187-37925325 | Rare:52 | ||||
chr2:37925437-37925538 | Rare:39 | ||||
chr2:38073322-38073480 | Rare:31 |