Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:78139590-78139779 | Common:3; Rare:76; Clinvar:2 | ||||
chr11:83071809-83072111 | Common:4; Rare:86 | ||||
chr11:83193604-83193755 | Common:1; Rare:68 | ||||
chr11:85628340-85628673 | Common:6; Rare:110 | ||||
chr11:85647891-85648036 | Common:1; Rare:39; Clinvar:2; Clinvar (benign):1 | ||||
chr11:86069851-86069939 | Common:1; Rare:15 | ||||
chr11:86244971-86245263 | Common:1; Rare:127 | ||||
chr11:88337598-88337888 | Common:4; Rare:137; Clinvar:7; Clinvar (benign):3 | ||||
chr11:90222966-90223195 | Common:2; Rare:96 | ||||
chr11:93741432-93741695 | Common:5; Rare:110 | ||||
chr11:93783967-93784362 | Common:6; Rare:113 | ||||
chr11:94493750-94494072 | Common:6; Rare:93; Clinvar:1; Clinvar (benign):2 | ||||
chr11:94973535-94973719 | Rare:54 | ||||
chr11:95789479-95789714 | Common:2; Rare:110 | ||||
chr11:95790329-95790704 | Common:3; Rare:145 |