Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:92291022-92291352 | Common:5; Rare:106 | ||||
chr10:92574007-92574149 | Common:1; Rare:44 | ||||
chr10:93702432-93702719 | Common:5; Rare:99 | ||||
chr10:95656652-95656920 | Rare:74; Clinvar:5 | ||||
chr10:95693879-95694219 | Common:5; Rare:111; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr10:95907850-95907955 | Common:2; Rare:34 | ||||
chr10:96129969-96130522 | Common:5; Rare:185 | ||||
chr10:96832055-96832302 | Rare:98 | ||||
chr10:97334690-97334830 | Common:1; Rare:61 | ||||
chr10:97425912-97426258 | Common:15; Rare:145 | ||||
chr10:97445983-97446217 | Rare:60 | ||||
chr10:97498368-97498569 | Common:2; Rare:83 | ||||
chr10:97633434-97633612 | Common:2; Rare:43 | ||||
chr10:97687223-97687545 | Common:5; Rare:97 | ||||
chr10:98268183-98268480 | Common:3; Rare:75 |