Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:77191480-77191940 | Common:6; Rare:89 | ||||
chr11:77192081-77192303 | Common:1; Rare:83; Clinvar:7; Clinvar (benign):3; Clinvar (pathogenic):6 | ||||
chr11:77300126-77300291 | Common:6; Rare:35 | ||||
chr11:77638434-77638544 | Rare:16 | ||||
chr11:77735001-77735401 | Common:4; Rare:133 | ||||
chr11:77819450-77819578 | Rare:36 | ||||
chr11:78000273-78000392 | Common:1; Rare:21 | ||||
chr11:78040066-78040242 | Rare:32 | ||||
chr11:78041026-78041223 | Common:2; Rare:45 | ||||
chr11:78416401-78416564 | Rare:50 | ||||
chr11:78416832-78417232 | Common:12; Rare:155 | ||||
chr11:83151585-83151836 | Common:1; Rare:45 | ||||
chr11:85759860-85760210 | Common:2; Rare:69 | ||||
chr11:85844515-85844672 | Common:1; Rare:37 | ||||
chr11:86193452-86193695 | Common:4; Rare:54 |