Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr12:132887558-132887779 | Rare:69 | ||||
chr12:132956260-132956370 | Common:1; Rare:26 | ||||
chr12:133130234-133130611 | Common:7; Rare:116 | ||||
chr13:19863639-19863939 | Common:3; Rare:115 | ||||
chr13:20773923-20774032 | Rare:36 | ||||
chr13:21176544-21176699 | Common:1; Rare:76 | ||||
chr13:24512727-24512839 | Common:3; Rare:34 | ||||
chr13:26221822-26221932 | Rare:27 | ||||
chr13:27251283-27251678 | Common:4; Rare:109 | ||||
chr13:27450119-27450215 | Common:3; Rare:29 | ||||
chr13:28659042-28659184 | Rare:65; Clinvar (pathogenic):1 | ||||
chr13:30306974-30307198 | Common:5; Rare:53 | ||||
chr13:30906579-30906728 | Common:2; Rare:44 | ||||
chr13:32586252-32586582 | Common:2; Rare:100 | ||||
chr13:33285703-33286038 | Common:1; Rare:66 |