Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:10353597-10353925 | Common:3; Rare:117 | ||||
chr5:14664579-14664914 | Common:3; Rare:137 | ||||
chr5:16465217-16465397 | Rare:58 | ||||
chr5:16465689-16465895 | Rare:43 | ||||
chr5:31532037-31532352 | Common:3; Rare:88 | ||||
chr5:31855053-31855123 | Common:1; Rare:23 | ||||
chr5:32174252-32174402 | Common:1; Rare:57 | ||||
chr5:32710453-32710675 | Common:1; Rare:42 | ||||
chr5:33440606-33441071 | Common:6; Rare:122 | ||||
chr5:34915486-34915741 | Common:1; Rare:59 | ||||
chr5:36151819-36152120 | Rare:74 | ||||
chr5:36876639-36876960 | Common:1; Rare:92; Clinvar:1; Clinvar (benign):3 | ||||
chr5:36876996-36877155 | Rare:53; Clinvar:1; Clinvar (benign):1 | ||||
chr5:38557231-38557391 | Rare:46 | ||||
chr5:38845769-38846053 | Common:1; Rare:73 |