Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:74170845-74171427 | Common:3; Rare:186 | ||||
chr11:74398410-74398558 | Common:3; Rare:36 | ||||
chr11:74467439-74467640 | Common:4; Rare:45; Clinvar (benign):1 | ||||
chr11:74592457-74592688 | Common:1; Rare:72 | ||||
chr11:74949055-74949301 | Common:6; Rare:69 | ||||
chr11:75351610-75351878 | Common:3; Rare:80 | ||||
chr11:75668626-75668773 | Rare:35 | ||||
chr11:76381125-76381410 | Common:4; Rare:98 | ||||
chr11:76444598-76444923 | Rare:82 | ||||
chr11:76669952-76670063 | Rare:19 | ||||
chr11:76783052-76783381 | Common:10; Rare:111 | ||||
chr11:77637665-77637868 | Common:1; Rare:74 | ||||
chr11:77820811-77821210 | Common:2; Rare:116 | ||||
chr11:78079610-78079654 | Rare:12 | ||||
chr11:78079690-78079985 | Common:2; Rare:90 |