Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:241944952-241945052 | Rare:19 | ||||
chr1:244451126-244451257 | Common:2; Rare:37 | ||||
chr1:244833869-244834019 | Common:1; Rare:34 | ||||
chr1:244863664-244863924 | Rare:88; Clinvar:3; Clinvar (benign):5 | ||||
chr1:246304652-246304815 | Common:4; Rare:24 | ||||
chr1:246304927-246305155 | Rare:30 | ||||
chr1:246306728-246306920 | Common:3; Rare:26 | ||||
chr1:246307496-246307559 | Common:1; Rare:12 | ||||
chr1:246319219-246319342 | Rare:19 | ||||
chr1:246726370-246726598 | Common:3; Rare:40 | ||||
chr1:247210774-247211005 | Common:3; Rare:66 | ||||
chr10:1961121-1961268 | Common:1; Rare:24 | ||||
chr10:2545430-2545483 | Common:1; Rare:21 | ||||
chr10:3096960-3097078 | Common:7; Rare:9 | ||||
chr10:4991828-4991986 | Common:1; Rare:18 |