Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:47343019-47343360 | Common:1; Rare:115; Clinvar:10; Clinvar (benign):10; Clinvar (pathogenic):8 | ||||
chr11:47346180-47346644 | Common:3; Rare:122; Clinvar:19; Clinvar (benign):10; Clinvar (pathogenic):12 | ||||
chr11:47349772-47350077 | Common:4; Rare:116; Clinvar:27; Clinvar (benign):20; Clinvar (pathogenic):5 | ||||
chr11:47351769-47351861 | Rare:19 | ||||
chr11:65420029-65420168 | Rare:34 | ||||
chr11:65422688-65422804 | Common:1; Rare:36 | ||||
chr11:65455106-65455296 | Rare:87 | ||||
chr11:65489336-65489589 | Common:1; Rare:61 | ||||
chr11:65499010-65499753 | Common:3; Rare:450 | ||||
chr11:65505566-65505710 | Rare:69 | ||||
chr11:66062782-66063089 | Rare:54 | ||||
chr11:66346917-66346952 | Rare:8 | ||||
chr11:73182853-73183150 | Common:1; Rare:59 | ||||
chr11:73309353-73309632 | Common:1; Rare:93 | ||||
chr11:86955987-86956128 | Common:1; Rare:40 |