Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:15097291-15097421 | Common:2; Rare:64 | ||||
chr10:17201615-17201776 | Common:2; Rare:55 | ||||
chr10:17230589-17230711 | Rare:50; Clinvar:1 | ||||
chr10:17233585-17233930 | Common:3; Rare:110; Clinvar (benign):1 | ||||
chr10:17617287-17617534 | Common:4; Rare:88 | ||||
chr10:17643866-17644339 | Common:3; Rare:152 | ||||
chr10:18651521-18651663 | Common:1; Rare:49 | ||||
chr10:18659233-18659517 | Common:2; Rare:96 | ||||
chr10:18659601-18659664 | Rare:26 | ||||
chr10:18659749-18659831 | Rare:20 | ||||
chr10:21497139-21497318 | Common:1; Rare:35 | ||||
chr10:21534011-21534241 | Common:1; Rare:75 | ||||
chr10:21673944-21674277 | Rare:60 | ||||
chr10:22316116-22316462 | Common:3; Rare:133 | ||||
chr10:22321560-22321600 | Rare:10 |