Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:178413669-178414001 | Common:2; Rare:95 | ||||
chr2:178437425-178437690 | Rare:48 | ||||
chr2:179950718-179950852 | Common:1; Rare:39 | ||||
chr2:188994040-188994278 | Rare:58; Clinvar:5; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
chr2:188994546-188994778 | Common:1; Rare:63; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):3 | ||||
chr2:189004002-189004363 | Rare:107; Clinvar:7; Clinvar (benign):8; Clinvar (pathogenic):22 | ||||
chr2:190912752-190912996 | Common:2; Rare:49 | ||||
chr2:190918429-190918486 | Rare:13 | ||||
chr2:202037079-202037153 | Rare:7 | ||||
chr2:202037376-202037527 | Rare:18 | ||||
chr2:202376079-202376364 | Rare:118 | ||||
chr2:206161241-206161371 | Rare:34 | ||||
chr2:207239375-207239660 | Rare:44 | ||||
chr2:216372796-216372971 | Rare:33 | ||||
chr2:231455234-231455474 | Common:1; Rare:102 |