Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:22625808-22626002 | Common:2; Rare:68; Clinvar:2; Clinvar (benign):1 | ||||
chr11:26994040-26994180 | Common:1; Rare:23 | ||||
chr11:27363097-27363274 | Rare:85 | ||||
chr11:27506738-27506897 | Common:1; Rare:68 | ||||
chr11:28108115-28108414 | Common:1; Rare:90 | ||||
chr11:30322944-30323175 | Common:1; Rare:68 | ||||
chr11:31369737-31369882 | Rare:45 | ||||
chr11:31509575-31509796 | Common:1; Rare:71 | ||||
chr11:32583663-32583929 | Rare:95 | ||||
chr11:33015780-33015923 | Common:1; Rare:53 | ||||
chr11:33161449-33161657 | Common:6; Rare:55 | ||||
chr11:33257134-33257427 | Common:3; Rare:94 | ||||
chr11:33736391-33736596 | Common:2; Rare:64 | ||||
chr11:33774472-33774685 | Common:2; Rare:76 | ||||
chr11:34051631-34051741 | Rare:51 |