Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:42142501-42142716 | Common:1; Rare:54 | ||||
chr6:42746062-42746348 | Rare:84 | ||||
chr6:42879594-42879940 | Rare:100 | ||||
chr6:42929046-42929175 | Rare:31 | ||||
chr6:42929209-42929571 | Common:4; Rare:108 | ||||
chr6:42929668-42929834 | Common:1; Rare:57 | ||||
chr6:42960613-42960972 | Common:1; Rare:95; Clinvar (pathogenic):1 | ||||
chr6:42984300-42984604 | Rare:73 | ||||
chr6:43013908-43014280 | Common:1; Rare:77 | ||||
chr6:43053766-43054008 | Common:2; Rare:80; Clinvar:5; Clinvar (benign):1 | ||||
chr6:43427426-43427599 | Rare:46 | ||||
chr6:43516887-43517113 | Common:4; Rare:85; Clinvar:2; Clinvar (benign):1 | ||||
chr6:43575962-43576186 | Rare:87; Clinvar:4 | ||||
chr6:43629143-43629437 | Common:2; Rare:87 | ||||
chr6:43687744-43688026 | Common:2; Rare:89 |