Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:86955331-86955694 | Common:1; Rare:122; Clinvar:2; Clinvar (benign):1 | ||||
chr11:87037686-87038166 | Common:3; Rare:200 | ||||
chr11:88175423-88175579 | Common:1; Rare:62 | ||||
chr11:88337590-88337905 | Common:5; Rare:146; Clinvar:7; Clinvar (benign):3 | ||||
chr11:90134518-90134765 | Common:1; Rare:70 | ||||
chr11:90223005-90223442 | Common:3; Rare:133 | ||||
chr11:93197396-93197598 | Common:1; Rare:45 | ||||
chr11:93197860-93198020 | Common:2; Rare:57 | ||||
chr11:93543118-93543139 | Rare:3 | ||||
chr11:93543374-93543610 | Common:3; Rare:51 | ||||
chr11:93661435-93661825 | Common:1; Rare:104 | ||||
chr11:93661935-93662107 | Rare:41 | ||||
chr11:93740663-93741005 | Common:2; Rare:86 | ||||
chr11:93741184-93741352 | Common:1; Rare:52 | ||||
chr11:93741377-93741913 | Common:7; Rare:171 |