Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:58575785-58576213 | Common:2; Rare:90 | ||||
chr11:58578074-58578522 | Common:4; Rare:141 | ||||
chr11:58905285-58905398 | Common:1; Rare:22 | ||||
chr11:59142743-59143302 | Common:2; Rare:107 | ||||
chr11:59615880-59616172 | Rare:75 | ||||
chr11:59668950-59669316 | Rare:131 | ||||
chr11:60906383-60906622 | Common:1; Rare:65 | ||||
chr11:60951777-60951807 | Rare:5 | ||||
chr11:61316367-61316517 | Common:1; Rare:36 | ||||
chr11:61333002-61333275 | Common:1; Rare:98 | ||||
chr11:61361837-61362038 | Common:1; Rare:49 | ||||
chr11:61362206-61362314 | Common:1; Rare:37; Clinvar:3; Clinvar (benign):1 | ||||
chr11:61362321-61362412 | Rare:20; Clinvar:4 | ||||
chr11:61429829-61430155 | Common:1; Rare:135; Clinvar:2; Clinvar (benign):4 | ||||
chr11:61792556-61792961 | Common:6; Rare:116 |