chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1171006637171006638AAG14GENICpossibly homozygous60941889
1171006648171006650AA--18GENICheterozygous60941890
1171006649171006650AAG18GENICpossibly homozygous60941891
1171006659171006660AG23GENICheterozygous60941892
1171006678171006679AAG16GENICheterozygous60941893
1171006679171006680AAG11GENICpossibly homozygous60941894
1171006737171006738GGA7GENIChomozygous60941895
1171008278171008279CCA20GENICheterozygous60941896
1171009499171009500GA28GENIChomozygous60941897
1171009908171009909GGAAA26GENICpossibly homozygous60941898
1171009908171009909GGA26GENICheterozygous60941899
1171009932171009933AG50GENICheterozygous60941900
1171010074171010075AG39GENIChomozygous60941901
1171010251171010252GA45GENIChomozygous60941902
1171010379171010380GT65GENIChomozygous60941903
1171010472171010474AA--3GENIChomozygous60941904
1171010621171010622GA47GENIChomozygous60941905
1171015917171015918CCA36GENIChomozygous60941906