Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:59429791-59429891 | Common:1; Rare:12 | ||||
chr1:62287029-62287157 | Rare:25 | ||||
chr1:62299843-62300178 | Common:2; Rare:64 | ||||
chr1:62327486-62327581 | Rare:24 | ||||
chr1:62327937-62328145 | Common:2; Rare:35 | ||||
chr1:62384694-62384828 | Rare:18 | ||||
chr1:63638569-63638781 | Common:3; Rare:66; Clinvar:2 | ||||
chr1:63654102-63654381 | Common:5; Rare:64; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr1:67686764-67686937 | Rare:28 | ||||
chr1:67832050-67832224 | Common:1; Rare:40 | ||||
chr1:87155899-87156029 | Rare:33 | ||||
chr1:88647301-88647539 | Common:2; Rare:46 | ||||
chr1:108816470-108816753 | Common:2; Rare:69 | ||||
chr1:109099958-109100236 | Common:3; Rare:109 | ||||
chr1:109530401-109530810 | Common:3; Rare:88 |