chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5137253641137253642GA39GENIChomozygous137632602
5137253876137253877TA57GENIChomozygous137632603
5137254142137254143TG45GENIChomozygous137632604
5137255545137255546TC56GENIChomozygous137632605
5137259381137259382TC32GENIChomozygous143963586
5137259381137259382T32GENICheterozygous403159786
5137259956137259957CT39GENIChomozygous137632606
5137261171137261172GT44GENIChomozygous137632607
5137268262137268263CT59GENIChomozygous137632609
5137268361137268362CT56GENIChomozygous137632610
5137268802137268803TG52GENIChomozygous137632611
5137269102137269103TC39GENIChomozygous137632612
5137269274137269275CT44GENIChomozygous137632613
5137271910137271911GA38GENIChomozygous137632614
5137272231137272232AG50GENIChomozygous137632616
5137272699137272700CT40GENIChomozygous137632617
5137272719137272720CA39GENIChomozygous137632618
5137273040137273041TA51GENIChomozygous137632619
5137273079137273080AG36GENIChomozygous137632620
5137273246137273247AT53GENIChomozygous137632621
5137273247137273248AT53GENIChomozygous137632622
5137272535137272537CA27GENIChomozygous137344494
5137259385137259385TCT31GENIChomozygous143944808