Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:62537682-62537949 | Common:1; Rare:45; Clinvar:1 | ||||
chr1:62548305-62548363 | Common:1; Rare:11 | ||||
chr1:62625372-62625597 | Rare:50; Clinvar:1; Clinvar (benign):1 | ||||
chr1:62747742-62747819 | Rare:12 | ||||
chr1:63436736-63436932 | Common:2; Rare:45; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr1:63438845-63439087 | Common:3; Rare:58 | ||||
chr1:63731693-63731971 | Common:2; Rare:48 | ||||
chr1:63780192-63780446 | Common:1; Rare:40 | ||||
chr1:63782576-63782892 | Rare:59 | ||||
chr1:63788665-63788773 | Rare:16 | ||||
chr1:63806567-63806644 | Rare:26 | ||||
chr1:64828132-64828245 | Common:2; Rare:25 | ||||
chr1:64872331-64872476 | Rare:26 | ||||
chr1:64872931-64873145 | Common:2; Rare:32 | ||||
chr1:64884782-64884943 | Rare:26 |