Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:26432079-26432439 | Common:5; Rare:94; Clinvar:2; Clinvar (benign):1 | ||||
chr1:26472260-26472535 | Common:4; Rare:92 | ||||
chr1:26787870-26788214 | Common:3; Rare:98; Clinvar:2; Clinvar (benign):2 | ||||
chr1:26900429-26900533 | Rare:38 | ||||
chr1:26921554-26921869 | Common:3; Rare:99 | ||||
chr1:27604079-27604528 | Common:2; Rare:131 | ||||
chr1:27725679-27725996 | Common:2; Rare:92 | ||||
chr1:27772921-27773373 | Common:1; Rare:147 | ||||
chr1:27830662-27830841 | Common:3; Rare:61 | ||||
chr1:28088546-28088801 | Common:3; Rare:87 | ||||
chr1:28176657-28176991 | Common:2; Rare:57 | ||||
chr1:28235963-28236264 | Common:3; Rare:95 | ||||
chr1:28328908-28329069 | Common:1; Rare:49 | ||||
chr1:28369557-28369807 | Common:3; Rare:98 | ||||
chr1:28505823-28506050 | Common:2; Rare:89 |