Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:59296508-59297103 | Common:14; Rare:166 | ||||
chr1:61742325-61742549 | Rare:65 | ||||
chr1:62319193-62319383 | Common:2; Rare:53 | ||||
chr1:62688274-62688517 | Common:1; Rare:95 | ||||
chr1:63322405-63322663 | Common:1; Rare:78 | ||||
chr1:63367522-63367694 | Rare:53; Clinvar (benign):1 | ||||
chr1:63523194-63523584 | Common:3; Rare:100 | ||||
chr1:64966375-64966714 | Common:2; Rare:118 | ||||
chr1:66924800-66925086 | Rare:116 | ||||
chr1:66925192-66925503 | Common:2; Rare:97 | ||||
chr1:66930088-66930426 | Rare:110 | ||||
chr1:67684919-67685177 | Common:2; Rare:62 | ||||
chr1:67833342-67833573 | Common:3; Rare:89 | ||||
chr1:70205527-70205759 | Rare:81 | ||||
chr1:70354692-70354856 | Rare:61 |