Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:83193629-83193788 | Common:1; Rare:72 | ||||
chr11:83285944-83286130 | Common:2; Rare:85 | ||||
chr11:83286331-83286518 | Rare:48 | ||||
chr11:85719166-85719466 | Common:2; Rare:60 | ||||
chr11:87037793-87038048 | Common:2; Rare:120 | ||||
chr11:88337661-88337888 | Common:4; Rare:109; Clinvar:6; Clinvar (benign):3 | ||||
chr11:90223015-90223128 | Common:1; Rare:43 | ||||
chr11:93741343-93741695 | Common:7; Rare:142 | ||||
chr11:94493789-94494029 | Common:3; Rare:68; Clinvar (benign):1 | ||||
chr11:94973535-94973843 | Rare:80 | ||||
chr11:95790369-95790541 | Rare:68 | ||||
chr11:95923955-95924164 | Rare:88; Clinvar (benign):1 | ||||
chr11:96389862-96390067 | Common:1; Rare:84 | ||||
chr11:102347137-102347254 | Common:1; Rare:31 | ||||
chr11:102452619-102452943 | Common:2; Rare:101 |