chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2196602531196602532AT9GENICheterozygous135259452
2196602533196602534AT8GENICheterozygous135259453
2196602535196602536AT8GENICheterozygous135259454
2196602537196602538AT7GENICheterozygous135259455
2196604895196604896CG29GENIChomozygous111154038
2196605726196605727AG29GENIChomozygous110996405
2196607532196607532T17GENICpossibly homozygous134800848
2196607918196607918A15GENIChomozygous127722639
2196607942196607943C13GENIChomozygous127722640
2196607950196607950C11GENIChomozygous127722641
2196607960196607960T11GENIChomozygous127722642
2196607964196607964C11GENIChomozygous127722643
2196607970196607970A10GENIChomozygous127722644
2196608048196608049A20GENIChomozygous127722645
2196608054196608054A20GENIChomozygous127722646
2196608093196608094T3GENIChomozygous127722647
2196609411196609412TC23GENIChomozygous110196089
2196611745196611746CT17GENIChomozygous110996407
2196612473196612477TCTG16GENICpossibly homozygous127722648
2196620256196620260TGTA17GENIChomozygous130873992
2196639812196639812A8GENIChomozygous134800849
2196639841196639841A9GENIChomozygous127722650
2196639858196639859G11GENIChomozygous127722651
2196639872196639872G12GENIChomozygous127722652
2196640617196640617A18GENIChomozygous134800850
2196619818196619819GA23GENIChomozygous120447559
2196619074196619075CT19GENIChomozygous110196090
2196624047196624048GA17GENIChomozygous110996409
2196628341196628342CT6GENIChomozygous127831290