Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:28846270-28846689 | Common:2; Rare:137; Clinvar:5; Clinvar (benign):5 | ||||
chr16:28925162-28925306 | Rare:44 | ||||
chr16:29805336-29805760 | Common:2; Rare:199 | ||||
chr16:29863213-29863549 | Common:1; Rare:85 | ||||
chr16:29995606-29995701 | Rare:43 | ||||
chr16:29996070-29996271 | Common:2; Rare:71 | ||||
chr16:30069574-30070005 | Common:1; Rare:161; Clinvar:6; Clinvar (benign):7 | ||||
chr16:30355219-30355434 | Common:1; Rare:76 | ||||
chr16:31472105-31472191 | Rare:23 | ||||
chr16:31508371-31508430 | Rare:26 | ||||
chr16:46689129-46689310 | Common:1; Rare:72; Clinvar:2; Clinvar (benign):1 | ||||
chr16:46689520-46689728 | Common:2; Rare:91; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr16:46973657-46973772 | Rare:52 | ||||
chr16:47461051-47461343 | Common:2; Rare:98; Clinvar (benign):1 | ||||
chr16:50152862-50152946 | Rare:32 |