Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:28846271-28846623 | Common:2; Rare:121; Clinvar:5; Clinvar (benign):5 | ||||
chr16:28878251-28878595 | Common:2; Rare:76 | ||||
chr16:28879744-28880015 | Common:2; Rare:72 | ||||
chr16:28887221-28887491 | Common:1; Rare:88; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
chr16:28925172-28925379 | Rare:68 | ||||
chr16:28974548-28974792 | Common:2; Rare:81 | ||||
chr16:29790578-29790757 | Rare:64 | ||||
chr16:29807876-29808131 | Common:1; Rare:155 | ||||
chr16:29961968-29962161 | Common:1; Rare:62 | ||||
chr16:29995606-29995704 | Rare:43 | ||||
chr16:29996064-29996296 | Common:2; Rare:82 | ||||
chr16:30065555-30065921 | Rare:128 | ||||
chr16:30069659-30070029 | Common:1; Rare:129; Clinvar:3; Clinvar (benign):7 | ||||
chr16:30075883-30076034 | Rare:50 | ||||
chr16:30123073-30123342 | Common:5; Rare:78 |