Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:130914521-130914571 | Rare:19 | ||||
chr11:130915248-130915302 | Rare:16 | ||||
chr11:131896705-131896873 | Rare:38 | ||||
chr11:134069737-134069811 | Common:1; Rare:20 | ||||
chr11:134095351-134095532 | Rare:38 | ||||
chr11:134114264-134114529 | Common:3; Rare:69 | ||||
chr11:134140188-134140448 | Common:3; Rare:60 | ||||
chr11:134143949-134144387 | Common:4; Rare:144; Clinvar (pathogenic):1 | ||||
chr11:134145711-134146048 | Common:1; Rare:89; Clinvar (pathogenic):1 | ||||
chr11:134155041-134155128 | Common:1; Rare:29 | ||||
chr11:134203883-134204076 | Common:2; Rare:57 | ||||
chr11:134237487-134237657 | Common:1; Rare:30 | ||||
chr12:21332-21646 | Common:7; Rare:20 | ||||
chr12:336585-336746 | Common:3; Rare:30 | ||||
chr12:642741-642849 | Common:2; Rare:34 |