Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:90222998-90223128 | Common:1; Rare:50 | ||||
chr11:93197882-93198002 | Common:2; Rare:38 | ||||
chr11:93741380-93741711 | Common:7; Rare:132 | ||||
chr11:93784095-93784380 | Common:6; Rare:85 | ||||
chr11:94493789-94494053 | Common:4; Rare:77; Clinvar (benign):1 | ||||
chr11:94973517-94973688 | Rare:57 | ||||
chr11:95067035-95067194 | Rare:41 | ||||
chr11:95067448-95067590 | Rare:58 | ||||
chr11:95089725-95089930 | Common:3; Rare:89 | ||||
chr11:95789569-95789887 | Common:3; Rare:141 | ||||
chr11:95790359-95790610 | Common:1; Rare:96 | ||||
chr11:95923827-95924157 | Common:2; Rare:145; Clinvar:5; Clinvar (benign):5 | ||||
chr11:96342999-96343061 | Rare:10 | ||||
chr11:96389851-96390065 | Common:1; Rare:92 | ||||
chr11:101127541-101127722 | Rare:80 |