chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
162486311324863114CCGT19GENICpossibly homozygous736562848
162486313224863133TA25GENICpossibly homozygous615095773
162486320324863204TA32GENIChomozygous614096113
162486376124863762GA42GENIChomozygous615095774
162486389124863892GC30GENIChomozygous614096114
162486399024863991GGT20GENIChomozygous736562849
162486527524865276A-21GENIChomozygous736562850
162486561624865617CT27GENIChomozygous614096115
162486565224865664TCTTTCTTTCTT------------2GENIChomozygous736562853
162486670024866701TC17GENIChomozygous615095775
162486680224866803CT34GENIChomozygous615095776
162486702724867028CCT29GENIChomozygous736562854
162486775724867758AG32GENIChomozygous615095777
162486855024868551CT28GENIChomozygous614096116
162486918724869188CT28GENIChomozygous615095778
162486920124869202GA27GENIChomozygous615095779
162486940724869408TA26GENIChomozygous614096117
162486964924869653TAAG----22GENIChomozygous736562855
162486971724869718GC26GENIChomozygous615095780
162486974824869749A-25GENIChomozygous736562856
162487027424870275CG21GENIChomozygous615095781
162487138124871382GGT7GENICheterozygous736562857
162487154224871543TC2GENIChomozygous615095782
162487154424871545CG2GENIChomozygous615095783
162487169924871700CT21GENICpossibly homozygous615095784
162487173724871738CA10GENICheterozygous615095785