chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1245838754583876AG25GENIChomozygous50394814
1245841194584120AG23GENIChomozygous50394816
1245844164584428GTGTGTGTGAGT------------51GENIChomozygous50394818
1245844534584454CT52GENIChomozygous50394824
1245845474584565TGTGTGTGTGTGTGTGTG------------------31GENIChomozygous50503205
1245850194585020GA24GENIChomozygous50394826
1245852374585238TC17GENIChomozygous50394828
1245858854585917ACACACACACACACACACACACACACACACAC--------------------------------16GENIChomozygous50503206
1245865614586562AAGGACAGCCG20GENIChomozygous50394830
1245872024587203AG28GENIChomozygous50394832
1245875604587561T-14GENIChomozygous50394834
1245889194588920AC18GENIChomozygous50394840
1245889284588929CG19GENIChomozygous50394842
1245890814589082AC22GENIChomozygous50004423
1245891914589192TTTTG20GENICpossibly homozygous50394844
1245891944589195AT20GENIChomozygous50503207
1245893314589332TA16GENIChomozygous50394848
1245894284589429TA28GENIChomozygous50394850
1245896274589628CT18GENIChomozygous50004425
1245900844590085CT23GENICpossibly homozygous50394852
1245904804590481TC28GENIChomozygous50394854
1245907984590799A-11GENIChomozygous50004427
1245910444591045GGA13GENIChomozygous50394856
1245913484591349TA23GENIChomozygous50394858
1245915534591554AC28GENIChomozygous50394860
1245918364591837AG26GENIChomozygous50394862
1245920474592048CT27GENIChomozygous50394864
1245879204587921GGCACACACACA18GENICheterozygous50526641
1245879204587921GGCACACACACACA18GENICheterozygous50526643
1245886484588654ACACAC------16GENIChomozygous50526647