Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:47248791-47248941 | Rare:60 | ||||
chr11:47269531-47269714 | Common:1; Rare:62 | ||||
chr11:47270012-47270202 | Common:1; Rare:71 | ||||
chr11:47426402-47426725 | Common:1; Rare:73 | ||||
chr11:47565460-47565646 | Common:3; Rare:37 | ||||
chr11:47578947-47579089 | Rare:73; Clinvar:2 | ||||
chr11:47642461-47642807 | Rare:126 | ||||
chr11:57324883-57325183 | Common:1; Rare:100 | ||||
chr11:57335738-57335937 | Common:4; Rare:48 | ||||
chr11:57426885-57426992 | Rare:18 | ||||
chr11:57514847-57515005 | Rare:31 | ||||
chr11:57530682-57530843 | Common:1; Rare:41 | ||||
chr11:57567612-57567887 | Rare:81 | ||||
chr11:57597558-57597720 | Rare:39; Clinvar:3; Clinvar (benign):1 | ||||
chr11:57712013-57712629 | Common:10; Rare:206 |