chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2208072899208072900CT33GENIChomozygous59357047
2208073353208073354TTCCATATACACCCTCTTG16GENIChomozygous59357048
2208073495208073496CT30GENIChomozygous59357049
2208074158208074159CG31GENIChomozygous59357050
2208074165208074166AG34GENIChomozygous59357051
2208074433208074434CCAT41GENIChomozygous59357052
2208074623208074624CCA24GENIChomozygous59357053
2208074629208074630TC27GENIChomozygous59357054
2208075276208075277GA45GENIChomozygous59357056
2208075282208075283CT48GENIChomozygous59357057
2208075442208075443TC35GENIChomozygous59357058
2208075455208075456CT36GENIChomozygous59357059
2208076388208076389GA36GENIChomozygous59357060
2208076723208076724AG31GENIChomozygous59357061
2208076742208076743TG25GENIChomozygous59357062
2208076744208076745GA25GENIChomozygous59357063
2208076763208076764CCCA19GENIChomozygous59357064
2208076944208076945GA54GENIChomozygous59357065
2208077095208077096CT49GENIChomozygous59357066
2208077188208077189GGGTGTCGTAA24GENIChomozygous59357067
2208077504208077505GGTC35GENIChomozygous59357068
2208077961208077962AC25GENIChomozygous59357069
2208078079208078080TC41GENIChomozygous59357070
2208078159208078160AG49GENIChomozygous59357071
2208078390208078391TG48GENIChomozygous59357072
2208078484208078485AC34GENIChomozygous59357073
2208078599208078600CT50GENIChomozygous59357074
2208078953208078954TC30GENIChomozygous59357075
2208079540208079541TTC25GENIChomozygous59357076
2208079565208079566TTA9GENICpossibly homozygous59357077
2208079944208079945GA24GENIChomozygous59357078
2208080102208080103GA44GENIChomozygous59357079
2208080735208080736TC40GENIChomozygous59357080
2208081693208081701CCCCCCCC--------5GENIChomozygous59357081
2208082156208082157GC12GENICheterozygous59357082
2208082159208082160GT10GENICheterozygous59357083
2208082165208082166CT23GENICheterozygous60158811
2208082174208082175CCATT21GENICpossibly homozygous59357086