chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
191034059310340594CT58GENIChomozygous109633596
191034117810341179AC75GENIChomozygous109633598
191034130810341309AG50GENIChomozygous109764542
191034219110342192GA57GENIChomozygous109633600
191034284110342842AG64GENIChomozygous109633602
191034289110342892AG71GENIChomozygous109633604
191034577310345774CT42GENIChomozygous109633606
191034577810345779AG44GENIChomozygous109633608
191034826310348264TC40GENIChomozygous109633610
191034956710349568CT49GENIChomozygous109633612
191035045210350453GA66GENIChomozygous109633614
191035496710354968TC54GENIChomozygous109633616
191035502110355022TC46GENIChomozygous109633618
191035552610355527GA79GENICpossibly homozygous109633620
191035762910357630AG48GENIChomozygous109633622
191034663710346638GA24GENICpossibly homozygous119596277
191034810410348105AG24GENICheterozygous119596278
191035848210358483CT68GENIChomozygous109633624
191035900410359005GT48GENIChomozygous109633626
191035921210359213AG60GENIChomozygous109633628