Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:507113-507445 | Common:2; Rare:104 | ||||
chr11:533902-533982 | Rare:26; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr11:534416-534584 | Rare:44 | ||||
chr11:560694-561021 | Common:6; Rare:152 | ||||
chr11:576420-576591 | Rare:70 | ||||
chr11:615625-615692 | Rare:24 | ||||
chr11:615946-615980 | Rare:7 | ||||
chr11:694803-695083 | Common:1; Rare:141; Clinvar:3; Clinvar (benign):4 | ||||
chr11:695614-695821 | Rare:51 | ||||
chr11:721157-721340 | Rare:79 | ||||
chr11:747275-747578 | Rare:130; Clinvar:5; Clinvar (benign):1 | ||||
chr11:763574-763943 | Rare:157; Clinvar:3 | ||||
chr11:764063-764430 | Common:2; Rare:104; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr11:777403-777607 | Common:1; Rare:94 | ||||
chr11:809486-809591 | Rare:34 |