chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
162486311324863114CCGT28GENIChomozygous47351697
162486313224863133TA32GENICpossibly homozygous47748851
162486320324863204TA12GENIChomozygous47351698
162486376124863762GA20GENICpossibly homozygous47748852
162486389124863892GC23GENIChomozygous47351699
162486399024863991GGT28GENICpossibly homozygous47748853
162486527524865276A-19GENIChomozygous47351700
162486561624865617CT23GENIChomozygous47351702
162486565224865664TCTTTCTTTCTT------------8GENICpossibly homozygous48089413
162486670024866701TC27GENIChomozygous47748856
162486680224866803CT27GENIChomozygous47748857
162486702724867028CCT19GENIChomozygous47748858
162486775724867758AG25GENICpossibly homozygous47748859
162486855024868551CT13GENIChomozygous47351707
162486918724869188CT24GENIChomozygous47748860
162486920124869202GA21GENIChomozygous47748861
162486940724869408TA17GENIChomozygous47351708
162486964924869653TAAG----15GENIChomozygous47748862
162486971724869718GC26GENIChomozygous47748863
162486974824869749A-33GENIChomozygous47748864
162487027424870275CG25GENIChomozygous47748865
162487138124871382GGT10GENICheterozygous47993749
162487154224871543TC2GENIChomozygous47993750
162487154424871545CG2GENIChomozygous47993751
162487169924871700CT13GENICpossibly homozygous47748869
162487173724871738CA9GENICpossibly homozygous47748870