Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:27549892-27550170 | Common:2; Rare:104 | ||||
chr16:28491949-28492121 | Common:1; Rare:41; Clinvar:2; Clinvar (benign):2 | ||||
chr16:28822576-28822732 | Rare:57 | ||||
chr16:28823964-28824221 | Common:2; Rare:79 | ||||
chr16:28844698-28844978 | Rare:93; Clinvar:2; Clinvar (benign):4 | ||||
chr16:28846307-28846698 | Common:2; Rare:121; Clinvar:4; Clinvar (benign):2 | ||||
chr16:29816301-29816496 | Common:1; Rare:59 | ||||
chr16:29863100-29863578 | Common:1; Rare:123 | ||||
chr16:29926155-29926321 | Common:2; Rare:65 | ||||
chr16:29995590-29995706 | Common:1; Rare:53 | ||||
chr16:29996067-29996289 | Common:2; Rare:80 | ||||
chr16:30065566-30065867 | Rare:101 | ||||
chr16:30069543-30070007 | Common:1; Rare:169; Clinvar:6; Clinvar (benign):7 | ||||
chr16:30096168-30096412 | Rare:67 | ||||
chr16:30355219-30355433 | Common:1; Rare:75 |