chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2208072899208072900CT26GENICpossibly homozygous59357047
2208073353208073354TTCCATATACACCCTCTTG1GENIChomozygous59357048
2208073495208073496CT29GENICpossibly homozygous59357049
2208074158208074159CG8GENIChomozygous59357050
2208074165208074166AG11GENIChomozygous59357051
2208074433208074434CCAT31GENICpossibly homozygous59357052
2208074623208074624CCA12GENICpossibly homozygous59357053
2208074629208074630TC15GENICpossibly homozygous59357054
2208075011208075012GC20GENIChomozygous59357055
2208075276208075277GA11GENIChomozygous59357056
2208075282208075283CT8GENIChomozygous59357057
2208075442208075443TC11GENIChomozygous59357058
2208075455208075456CT16GENIChomozygous59357059
2208076388208076389GA23GENICpossibly homozygous59357060
2208076723208076724AG11GENIChomozygous59357061
2208076742208076743TG6GENIChomozygous59357062
2208076744208076745GA6GENIChomozygous59357063
2208076763208076764CCCA3GENIChomozygous59357064
2208076944208076945GA21GENICpossibly homozygous59357065
2208077095208077096CT25GENIChomozygous59357066
2208077188208077189GGGTGTCGTAA2GENIChomozygous59357067
2208077504208077505GGTC11GENIChomozygous59357068
2208077961208077962AC19GENIChomozygous59357069
2208078079208078080TC18GENICpossibly homozygous59357070
2208078159208078160AG22GENIChomozygous59357071
2208078390208078391TG12GENIChomozygous59357072
2208078484208078485AC12GENIChomozygous59357073
2208078599208078600CT18GENICpossibly homozygous59357074
2208078953208078954TC24GENIChomozygous59357075
2208079540208079541TTC6GENIChomozygous59357076
2208079944208079945GA14GENIChomozygous59357078
2208080102208080103GA20GENICpossibly homozygous59357079
2208080735208080736TC15GENICpossibly homozygous59357080
2208081693208081701CCCCCCCC--------1GENIChomozygous59357081