Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:102400663-102401027 | Common:3; Rare:88; Clinvar:2; Clinvar (benign):4 | ||||
chr10:102644901-102645078 | Rare:40 | ||||
chr10:102645104-102645189 | Rare:13 | ||||
chr10:102714277-102714638 | Common:2; Rare:122 | ||||
chr10:103193248-103193390 | Common:5; Rare:45; Clinvar (benign):1 | ||||
chr10:103396451-103396730 | Rare:96 | ||||
chr10:104121911-104122171 | Common:2; Rare:85 | ||||
chr10:104268964-104269208 | Common:3; Rare:59 | ||||
chr10:110008229-110008283 | Rare:24 | ||||
chr10:110008576-110008938 | Common:6; Rare:99 | ||||
chr10:110076919-110077096 | Common:1; Rare:30 | ||||
chr10:110304897-110305055 | Common:2; Rare:57 | ||||
chr10:110567419-110567744 | Common:2; Rare:80; Clinvar:1; Clinvar (benign):5 | ||||
chr10:110871814-110872015 | Rare:71 | ||||
chr10:110884320-110884413 | Rare:10 |