chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1234469950234469951GA26GENIChomozygous664600683
1234470515234470516CG24GENIChomozygous664600684
1234470893234470897TTTT----21GENIChomozygous765897822
1234470897234470898TC18GENIChomozygous664600685
1234471175234471176AT27GENIChomozygous664600686
1234472094234472095GA20GENIChomozygous664600687
1234472262234472263T-22GENIChomozygous765897823
1234472293234472294AT21GENIChomozygous664600688
1234472631234472632CT45GENIChomozygous664600689
1234475017234475018TC18GENIChomozygous664600690
1234475032234475033TC21GENIChomozygous664600691
1234475134234475135AAT28GENIChomozygous765897825
1234476652234476653AG29GENIChomozygous664600692
1234477038234477039TTAA19GENICpossibly homozygous765897827
1234477958234477968GTGTGTGTGT----------7GENIChomozygous765897828
1234480411234480412AAT8GENIChomozygous765897832
1234480510234480511GA41GENIChomozygous664600693
1234480571234480572AG30GENIChomozygous664600694
1234481486234481487TC20GENIChomozygous664600695
1234481606234481607GGCT17GENICpossibly homozygous765897833
1234481874234481875GA15GENIChomozygous664600696