Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:47767219-47767679 | Common:2; Rare:153 | ||||
chr11:47848322-47848406 | Rare:42 | ||||
chr11:57324883-57325169 | Common:1; Rare:95 | ||||
chr11:57338166-57338352 | Rare:29 | ||||
chr11:57427061-57427236 | Common:1; Rare:55 | ||||
chr11:57567612-57567746 | Rare:44 | ||||
chr11:57597407-57597720 | Rare:66; Clinvar:3; Clinvar (benign):1 | ||||
chr11:57657440-57657794 | Common:4; Rare:91 | ||||
chr11:57712013-57712630 | Common:10; Rare:206 | ||||
chr11:57741290-57741652 | Common:3; Rare:146 | ||||
chr11:57761616-57762018 | Common:3; Rare:80 | ||||
chr11:58578100-58578539 | Common:4; Rare:139 | ||||
chr11:58578951-58579192 | Common:2; Rare:62 | ||||
chr11:59142667-59142967 | Common:1; Rare:55 | ||||
chr11:59212889-59213125 | Common:1; Rare:64 |