Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:78139589-78139809 | Common:3; Rare:88; Clinvar:2 | ||||
chr11:78188592-78188938 | Common:2; Rare:109 | ||||
chr11:78574763-78574970 | Common:2; Rare:84; Clinvar (benign):1 | ||||
chr11:83071761-83072124 | Common:4; Rare:103 | ||||
chr11:83193608-83193786 | Common:1; Rare:82 | ||||
chr11:83285746-83286136 | Common:4; Rare:166 | ||||
chr11:83286330-83286479 | Rare:35 | ||||
chr11:83724920-83725021 | Rare:23 | ||||
chr11:85627770-85628061 | Common:1; Rare:57 | ||||
chr11:85628324-85628664 | Common:7; Rare:117 | ||||
chr11:85647808-85648005 | Rare:59; Clinvar:2 | ||||
chr11:85686133-85686389 | Common:2; Rare:54 | ||||
chr11:85811091-85811341 | Common:2; Rare:77 | ||||
chr11:86068653-86068877 | Rare:67 | ||||
chr11:86069037-86069177 | Rare:53 |