Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:77994644-77995165 | Common:3; Rare:155 | ||||
chr11:78079715-78079996 | Common:2; Rare:85 | ||||
chr11:78139574-78139882 | Common:3; Rare:108; Clinvar:2 | ||||
chr11:78188592-78188953 | Common:3; Rare:111 | ||||
chr11:78417664-78418140 | Common:3; Rare:189 | ||||
chr11:78574347-78574423 | Rare:30 | ||||
chr11:78574751-78575003 | Common:2; Rare:96; Clinvar (benign):1 | ||||
chr11:78962204-78962568 | Common:4; Rare:80 | ||||
chr11:79440945-79441196 | Common:1; Rare:78 | ||||
chr11:82900374-82900655 | Common:1; Rare:82 | ||||
chr11:83035516-83035789 | Common:1; Rare:38 | ||||
chr11:83071767-83072130 | Common:4; Rare:103 | ||||
chr11:83157009-83157212 | Rare:81 | ||||
chr11:83193604-83193765 | Common:1; Rare:73 | ||||
chr11:83285890-83286136 | Common:3; Rare:108 |