Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:182839207-182839402 | Common:1; Rare:82 | ||||
chr1:183023044-183023285 | Common:5; Rare:62 | ||||
chr1:183023932-183024094 | Rare:44 | ||||
chr1:183134655-183135155 | Common:3; Rare:116 | ||||
chr1:183635552-183636114 | Common:5; Rare:155 | ||||
chr1:184051627-184051768 | Common:3; Rare:55 | ||||
chr1:185156714-185156807 | Common:1; Rare:34 | ||||
chr1:185156900-185157309 | Common:2; Rare:113 | ||||
chr1:186375205-186375488 | Rare:67 | ||||
chr1:186375669-186375954 | Common:1; Rare:73 | ||||
chr1:193059190-193059768 | Common:1; Rare:250 | ||||
chr1:193121946-193122210 | Common:1; Rare:91; Clinvar:5; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr1:193186593-193186932 | Common:1; Rare:59 | ||||
chr1:201648564-201648667 | Rare:37 | ||||
chr1:201829084-201829234 | Rare:75 |