Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:70420112-70420411 | Common:4; Rare:65 | ||||
chr11:71448306-71448582 | Common:2; Rare:76; Clinvar:3; Clinvar (benign):1 | ||||
chr11:72041846-72041893 | Common:1; Rare:9 | ||||
chr11:72080399-72080745 | Common:2; Rare:80; Clinvar:7 | ||||
chr11:72814291-72814463 | Common:2; Rare:59 | ||||
chr11:73218205-73218290 | Rare:15 | ||||
chr11:73876778-73877024 | Common:5; Rare:66 | ||||
chr11:74170904-74171431 | Common:3; Rare:166 | ||||
chr11:74493711-74493786 | Rare:25 | ||||
chr11:74949062-74949288 | Common:6; Rare:59 | ||||
chr11:76783048-76783396 | Common:10; Rare:113 | ||||
chr11:77820924-77821210 | Common:1; Rare:86 | ||||
chr11:78139590-78139661 | Rare:29; Clinvar:2 | ||||
chr11:83071791-83072111 | Common:4; Rare:91 | ||||
chr11:83193624-83193804 | Common:1; Rare:84 |