Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:28822529-28822749 | Common:1; Rare:77 | ||||
chr16:28846256-28846696 | Common:2; Rare:146; Clinvar:6; Clinvar (benign):6 | ||||
chr16:28925159-28925269 | Rare:29 | ||||
chr16:28974552-28974792 | Common:2; Rare:80 | ||||
chr16:29454266-29454571 | |||||
chr16:29679006-29679190 | Rare:60 | ||||
chr16:29805486-29805641 | Common:1; Rare:73 | ||||
chr16:29815998-29816206 | Common:1; Rare:60 | ||||
chr16:29961968-29962163 | Common:1; Rare:63 | ||||
chr16:29995601-29995684 | Rare:39 | ||||
chr16:29996072-29996296 | Common:2; Rare:79 | ||||
chr16:30065457-30065897 | Rare:144 | ||||
chr16:30069660-30070022 | Common:1; Rare:127; Clinvar:3; Clinvar (benign):7 | ||||
chr16:30075889-30076055 | Rare:56 | ||||
chr16:30123058-30123378 | Common:6; Rare:93 |