Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:32805379-32805690 | Common:1; Rare:47 | ||||
chr22:32829168-32829469 | Common:2; Rare:62 | ||||
chr22:35376937-35377159 | Common:1; Rare:48 | ||||
chr22:36288725-36289194 | Common:2; Rare:139; Clinvar:4; Clinvar (benign):7 | ||||
chr22:36306455-36306713 | Common:1; Rare:84; Clinvar:1; Clinvar (benign):2 | ||||
chr22:36520587-36520772 | Common:1; Rare:47 | ||||
chr22:38682759-38682986 | Rare:48 | ||||
chr22:38741552-38741813 | Common:1; Rare:54 | ||||
chr22:38954033-38954067 | Rare:4 | ||||
chr22:39521530-39521828 | Common:1; Rare:141 | ||||
chr22:40651736-40651874 | Common:3; Rare:34 | ||||
chr22:41325574-41325817 | Rare:62 | ||||
chr22:41393655-41394009 | Common:5; Rare:77 | ||||
chr22:41413729-41414083 | Common:2; Rare:107 | ||||
chr22:41444411-41444579 | Common:2; Rare:37 |