Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:129815689-129815912 | Common:1; Rare:57 | ||||
chr11:130002760-130002954 | Common:3; Rare:39 | ||||
chr11:130069638-130070079 | Common:2; Rare:155 | ||||
chr11:130189738-130190142 | Common:3; Rare:139; Clinvar:1 | ||||
chr11:130314395-130314509 | Common:1; Rare:37 | ||||
chr11:130448527-130448647 | Rare:31 | ||||
chr11:130916281-130916631 | Common:8; Rare:98 | ||||
chr11:134224533-134224698 | Rare:63 | ||||
chr11:134225441-134225732 | Rare:79 | ||||
chr11:134253261-134253592 | Common:2; Rare:109; Clinvar (benign):1 | ||||
chr11:134331652-134331968 | Common:9; Rare:61 | ||||
chr12:388974-388993 | Rare:7 | ||||
chr12:389230-389383 | Rare:60 | ||||
chr12:401446-401664 | Rare:58 | ||||
chr12:460206-460505 | Common:2; Rare:76 |