Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:28846222-28846707 | Common:2; Rare:161; Clinvar:7; Clinvar (benign):6 | ||||
chr16:28863692-28863871 | Common:1; Rare:59 | ||||
chr16:28878627-28878786 | Common:1; Rare:58; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
chr16:28879679-28879789 | Rare:31 | ||||
chr16:28879853-28880094 | Common:3; Rare:75 | ||||
chr16:28880366-28880494 | Common:1; Rare:26 | ||||
chr16:28925167-28925241 | Rare:22 | ||||
chr16:28974669-28974792 | Rare:56 | ||||
chr16:29454308-29454590 | |||||
chr16:29995606-29995698 | Rare:43 | ||||
chr16:29996058-29996289 | Common:2; Rare:82 | ||||
chr16:30064098-30064783 | Common:2; Rare:127; Clinvar (benign):2 | ||||
chr16:30065324-30065923 | Rare:190 | ||||
chr16:30069495-30070029 | Common:1; Rare:199; Clinvar:6; Clinvar (benign):7 | ||||
chr16:30075894-30076034 | Rare:47 |