chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
162486311324863114CCGT14GENIChomozygous746469729
162486313224863133TA17GENIChomozygous632868702
162486320324863204TA28GENIChomozygous632868703
162486376124863762GA24GENIChomozygous632868704
162486389124863892GC15GENIChomozygous632868705
162486399024863991GGT16GENIChomozygous746469730
162486527524865276A-20GENIChomozygous746469731
162486561624865617CT25GENIChomozygous632868706
162486564424865664TCTTTCTTTCTTTCTTTCTT--------------------16GENIChomozygous746469733
162486670024866701TC25GENIChomozygous632868707
162486680224866803CT18GENIChomozygous632868708
162486702724867028CCT25GENICpossibly homozygous746469735
162486775724867758AG34GENIChomozygous632868709
162486855024868551CT26GENIChomozygous632868710
162486918724869188CT25GENIChomozygous632868711
162486920124869202GA28GENIChomozygous632868712
162486940724869408TA37GENIChomozygous632868713
162486964924869653TAAG----21GENIChomozygous746469736
162486971724869718GC15GENIChomozygous632868714
162486974824869749A-15GENIChomozygous746469737
162487027424870275CG24GENICpossibly homozygous632868715
162487135524871356CG11GENIChomozygous632868716
162487138124871382GGT9GENICheterozygous746469738
162487154224871543TC14GENIChomozygous632868717
162487154424871545CG13GENIChomozygous632868718
162487156524871566TA9GENIChomozygous632868719
162487169924871700CT17GENIChomozygous632868720
162487173724871738CA13GENIChomozygous632868721