Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:72793655-72793808 | Common:1; Rare:43 | ||||
chr11:72814054-72814458 | Common:4; Rare:121 | ||||
chr11:73760625-73760735 | Common:2; Rare:30 | ||||
chr11:73760934-73761167 | Common:3; Rare:74 | ||||
chr11:73876778-73877036 | Common:5; Rare:73 | ||||
chr11:74170842-74171099 | Common:1; Rare:75 | ||||
chr11:74171162-74171452 | Common:2; Rare:98 | ||||
chr11:74398403-74398558 | Common:3; Rare:38 | ||||
chr11:74493746-74493778 | Rare:10 | ||||
chr11:74592486-74592677 | Common:1; Rare:63 | ||||
chr11:74949055-74949294 | Common:6; Rare:64 | ||||
chr11:75351610-75351870 | Common:3; Rare:76 | ||||
chr11:75562063-75562292 | Common:1; Rare:58; Clinvar:4; Clinvar (benign):2 | ||||
chr11:76380886-76381353 | Common:3; Rare:152 | ||||
chr11:76444641-76445104 | Common:1; Rare:111 |