chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1204965204204965205AG1GENIChomozygous61585345
1204966845204966846TC3GENIChomozygous61585348
1204967295204967296GA10GENIChomozygous61063783
1204967746204967747GA13GENIChomozygous61585349
1204968010204968011CT10GENICpossibly homozygous61585350
1204968272204968273AG9GENIChomozygous61063785
1204968479204968480CA17GENICpossibly homozygous61585351
1204969470204969471GA18GENIChomozygous61585352
1204969589204969590TC14GENICpossibly homozygous61063793
1204969788204969789AG13GENICpossibly homozygous61585353
1204970595204970596GA5GENIChomozygous61585355
1204971906204971907TC4GENICheterozygous61063807
1204972221204972222CT7GENICpossibly homozygous61585359
1204973168204973169GA19GENIChomozygous61585360
1204973256204973257CA3GENICheterozygous61585361
1204973808204973809AG13GENIChomozygous61063818
1204974068204974069GA22GENICpossibly homozygous61585363
1204974504204974505GA19GENICpossibly homozygous61585364
1204974627204974628AAC3GENICheterozygous61585365
1204975685204975686CA5GENICheterozygous61063834
1204977529204977530AG5GENIChomozygous61585367
1204977546204977552ACAGGC------1GENIChomozygous61585368
1204977816204977817CT7GENIChomozygous61585369
1204978449204978450GA18GENICpossibly homozygous61063849
1204974636204974637AC4GENICheterozygous62095798