Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:78139581-78139815 | Common:3; Rare:92; Clinvar:2 | ||||
chr11:78188592-78188907 | Common:2; Rare:103 | ||||
chr11:83071797-83072124 | Common:4; Rare:91 | ||||
chr11:83193629-83193786 | Common:1; Rare:71 | ||||
chr11:85628338-85628688 | Common:6; Rare:115 | ||||
chr11:85647851-85648036 | Common:1; Rare:50; Clinvar:2; Clinvar (benign):1 | ||||
chr11:86244502-86244801 | Common:1; Rare:76 | ||||
chr11:86245008-86245268 | Common:1; Rare:116 | ||||
chr11:86672158-86672256 | Rare:20 | ||||
chr11:86955365-86955653 | Common:1; Rare:90 | ||||
chr11:87037753-87038043 | Common:3; Rare:136 | ||||
chr11:88337613-88337851 | Common:4; Rare:118; Clinvar:7; Clinvar (benign):3 | ||||
chr11:90222982-90223124 | Common:1; Rare:55 | ||||
chr11:93543312-93543587 | Common:3; Rare:73 | ||||
chr11:93741381-93741702 | Common:7; Rare:131 |