Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:76380902-76381348 | Common:3; Rare:144 | ||||
chr11:76444654-76444923 | Rare:60 | ||||
chr11:76783062-76783357 | Common:9; Rare:96 | ||||
chr11:77637733-77637868 | Common:1; Rare:51 | ||||
chr11:77820989-77821209 | Common:1; Rare:67 | ||||
chr11:78079761-78079950 | Common:2; Rare:59 | ||||
chr11:78139581-78139842 | Common:3; Rare:99; Clinvar:2 | ||||
chr11:78188588-78188901 | Common:2; Rare:104 | ||||
chr11:83071735-83072111 | Common:4; Rare:106 | ||||
chr11:83193619-83193794 | Common:1; Rare:81 | ||||
chr11:85627313-85627412 | Rare:19 | ||||
chr11:85647893-85648045 | Common:1; Rare:42; Clinvar:2; Clinvar (benign):1 | ||||
chr11:87037772-87038040 | Common:3; Rare:125 | ||||
chr11:88337661-88337888 | Common:4; Rare:109; Clinvar:6; Clinvar (benign):3 | ||||
chr11:90222992-90223185 | Common:1; Rare:78 |