Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:21283639-21283801 | Common:3; Rare:49 | ||||
chr16:21303013-21303210 | Rare:40 | ||||
chr16:21599279-21599778 | Common:4; Rare:170 | ||||
chr16:21599780-21599934 | Rare:56 | ||||
chr16:21600195-21600267 | Rare:14 | ||||
chr16:21600269-21600285 | Rare:3 | ||||
chr16:21952927-21953417 | Common:1; Rare:116; Clinvar (benign):3 | ||||
chr16:22007602-22007727 | Common:2; Rare:36 | ||||
chr16:22007916-22008219 | Rare:98 | ||||
chr16:22205986-22206418 | Common:1; Rare:108 | ||||
chr16:22296975-22297138 | Common:4; Rare:73 | ||||
chr16:22297145-22297499 | Common:3; Rare:179 | ||||
chr16:22297661-22297744 | Rare:20 | ||||
chr16:22297776-22298020 | Common:1; Rare:62 | ||||
chr16:22374509-22374925 | Common:1; Rare:147 |