Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:43013831-43014295 | Common:2; Rare:117 | ||||
chr6:43516866-43517106 | Common:3; Rare:93; Clinvar:2 | ||||
chr6:43576024-43576185 | Rare:52; Clinvar:4 | ||||
chr6:44127342-44127645 | Common:4; Rare:87 | ||||
chr6:49463191-49463417 | Common:1; Rare:65; Clinvar:1; Clinvar (benign):1 | ||||
chr6:52995336-52995652 | Common:4; Rare:129 | ||||
chr6:75284722-75285021 | Common:1; Rare:83 | ||||
chr6:83193222-83193364 | Common:3; Rare:52 | ||||
chr6:87589965-87590163 | Common:2; Rare:81; Clinvar (benign):3 | ||||
chr6:100881291-100881400 | Common:3; Rare:47 | ||||
chr6:106629462-106629581 | Common:1; Rare:23 | ||||
chr6:110981963-110982094 | Common:2; Rare:63 | ||||
chr6:112087470-112087649 | Rare:50 | ||||
chr6:116279892-116280112 | Common:1; Rare:67 | ||||
chr6:122471779-122471921 | Common:2; Rare:39 |