Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:98446801-98447055 | Rare:72; Clinvar:1 | ||||
chr10:99430621-99430923 | Common:3; Rare:69 | ||||
chr10:99659256-99659575 | Common:2; Rare:80 | ||||
chr10:99732076-99732329 | Rare:93; Clinvar:3 | ||||
chr10:100185920-100186207 | Rare:109 | ||||
chr10:100286640-100286722 | Common:2; Rare:47 | ||||
chr10:100346911-100347454 | Common:3; Rare:122 | ||||
chr10:100529836-100530010 | Common:1; Rare:45 | ||||
chr10:100535796-100535955 | Common:6; Rare:66 | ||||
chr10:100912669-100913031 | Common:1; Rare:107 | ||||
chr10:100913330-100913450 | Rare:31 | ||||
chr10:100987248-100987599 | Common:1; Rare:126; Clinvar:1; Clinvar (benign):1 | ||||
chr10:101031102-101031275 | Common:1; Rare:41 | ||||
chr10:101061680-101061999 | Rare:48 | ||||
chr10:101588166-101588333 | Rare:70 |