chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
185607151256071514AG38GENIChomozygous131206310
185607168256071683TC39GENIChomozygous110542844
185607175656071757CG47GENIChomozygous110542846
185607184356071844CA41GENIChomozygous110542848
185607239256072396ATCC35GENIChomozygous131206311
185607242156072422CG35GENIChomozygous110542850
185607243056072431AG35GENIChomozygous110542852
185607246356072464AC22GENIChomozygous110542854
185607247456072476CA28GENIChomozygous131206312
185607334356073344AT43GENIChomozygous110542856
185607377756073778GA49GENIChomozygous110542858
185607379456073795CG53GENIChomozygous110542860
185607379856073799GA53GENIChomozygous110542862
185607380556073806AG53GENIChomozygous110542864
185607384756073848CT43GENIChomozygous110542866
185607393356073934CT40GENIChomozygous110542868
185607408656074087GA40GENIChomozygous110542870
185607177956071780T42GENICpossibly homozygous129540498
185607322956073230TA54GENIChomozygous110361007
185607617456076175TC37GENIChomozygous110361015
185607729356077294CA51GENIChomozygous110542872
185607872956078730TC51GENIChomozygous110361037
185608037556080379CTTC58GENIChomozygous129540500