Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:63592937-63593491 | Rare:149; Clinvar (benign):1 | ||||
chr1:63773838-63774245 | Rare:81 | ||||
chr1:63775012-63775219 | Rare:63 | ||||
chr1:64744858-64745159 | Common:2; Rare:95 | ||||
chr1:64879023-64879231 | Rare:56 | ||||
chr1:64966375-64966714 | Common:2; Rare:118 | ||||
chr1:65420340-65420785 | Common:6; Rare:124; Clinvar:2; Clinvar (benign):1 | ||||
chr1:65420905-65421281 | Rare:78 | ||||
chr1:65525072-65525391 | Common:3; Rare:62 | ||||
chr1:66331986-66332666 | Rare:147 | ||||
chr1:66354515-66354569 | Rare:8 | ||||
chr1:66354587-66354844 | Common:1; Rare:41 | ||||
chr1:66360646-66360831 | Common:1; Rare:22 | ||||
chr1:66367650-66367736 | Rare:14 | ||||
chr1:66367767-66367918 | Rare:42 |