chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5137253641137253642GA53GENIChomozygous137632602
5137253876137253877TA59GENIChomozygous137632603
5137254142137254143TG46GENIChomozygous137632604
5137255545137255546TC53GENIChomozygous137632605
5137259381137259382TC47GENIChomozygous143963586
5137259956137259957CT46GENIChomozygous137632606
5137261171137261172GT55GENIChomozygous137632607
5137268262137268263CT55GENIChomozygous137632609
5137268361137268362CT51GENIChomozygous137632610
5137268802137268803TG43GENIChomozygous137632611
5137269102137269103TC48GENIChomozygous137632612
5137269274137269275CT44GENIChomozygous137632613
5137271910137271911GA55GENIChomozygous137632614
5137272231137272232AG50GENIChomozygous137632616
5137272699137272700CT54GENIChomozygous137632617
5137272719137272720CA56GENIChomozygous137632618
5137273040137273041TA42GENICpossibly homozygous137632619
5137273079137273080AG35GENIChomozygous137632620
5137273246137273247AT48GENIChomozygous137632621
5137273247137273248AT47GENIChomozygous137632622
5137272535137272537CA31GENIChomozygous137344494
5137259381137259382T47GENICheterozygous403159786
5137259385137259385TCT37GENIChomozygous143944808