Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:75525865-75526021 | Common:2; Rare:42 | ||||
chr11:75562044-75562303 | Common:1; Rare:64; Clinvar:4; Clinvar (benign):2 | ||||
chr11:76380858-76381083 | Rare:75 | ||||
chr11:76381089-76381353 | Common:3; Rare:82 | ||||
chr11:76444660-76445104 | Common:1; Rare:103 | ||||
chr11:76783013-76783395 | Common:10; Rare:121 | ||||
chr11:77637592-77637858 | Common:1; Rare:90 | ||||
chr11:77820577-77820752 | Rare:76 | ||||
chr11:77820945-77821210 | Common:1; Rare:83 | ||||
chr11:78139590-78139803 | Common:3; Rare:86; Clinvar:2 | ||||
chr11:78188592-78188980 | Common:3; Rare:123 | ||||
chr11:78417773-78418057 | Common:1; Rare:109 | ||||
chr11:78574660-78574934 | Common:2; Rare:102; Clinvar (benign):1 | ||||
chr11:83071748-83072111 | Common:4; Rare:105 | ||||
chr11:83193621-83193804 | Common:1; Rare:85 |