Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:77820966-77821210 | Common:1; Rare:74 | ||||
chr11:78079740-78079942 | Common:2; Rare:62 | ||||
chr11:78139590-78139851 | Common:3; Rare:98; Clinvar:2 | ||||
chr11:78188592-78188912 | Common:2; Rare:103 | ||||
chr11:78574773-78574970 | Common:2; Rare:78; Clinvar (benign):1 | ||||
chr11:83071818-83072108 | Common:4; Rare:81 | ||||
chr11:83193619-83193804 | Common:1; Rare:87 | ||||
chr11:83285876-83286087 | Common:3; Rare:91 | ||||
chr11:83286334-83286371 | Rare:15 | ||||
chr11:84437575-84437733 | Rare:36 | ||||
chr11:85628326-85628626 | Common:7; Rare:98 | ||||
chr11:85664655-85664826 | Common:1; Rare:86 | ||||
chr11:86068936-86069207 | Common:2; Rare:90 | ||||
chr11:86244634-86244801 | Rare:49 | ||||
chr11:86245012-86245268 | Common:1; Rare:114 |