Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:61361843-61362051 | Common:2; Rare:49; Clinvar:2 | ||||
chr11:61362255-61362404 | Common:1; Rare:42; Clinvar:7 | ||||
chr11:61392523-61392654 | Common:2; Rare:45; Clinvar:3; Clinvar (benign):2 | ||||
chr11:61429913-61430167 | Common:1; Rare:116; Clinvar:3; Clinvar (benign):5 | ||||
chr11:61792566-61792955 | Common:5; Rare:106 | ||||
chr11:61816120-61816277 | Rare:33 | ||||
chr11:61891436-61891766 | Common:2; Rare:100 | ||||
chr11:61967313-61967783 | Common:3; Rare:177; Clinvar:4 | ||||
chr11:62123731-62124089 | Common:7; Rare:96 | ||||
chr11:62545572-62546013 | Common:1; Rare:99 | ||||
chr11:62591494-62591837 | Rare:114 | ||||
chr11:62601615-62601932 | Rare:101 | ||||
chr11:62621949-62622232 | Common:2; Rare:87 | ||||
chr11:62646577-62646819 | Common:1; Rare:95; Clinvar (pathogenic):1 | ||||
chr11:62653262-62653510 | Common:1; Rare:75 |