chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
176969592869695929AT7GENIChomozygous791677625
176969781969697820GA16GENIChomozygous791677626
176969798469697985CT14GENIChomozygous791677627
176969870469698705TC16GENIChomozygous791677628
176969885769698858AG20GENIChomozygous791677629
176969939669699397GA11GENIChomozygous791677630
176969940469699405TG12GENIChomozygous791677631
176969950369699504AG9GENIChomozygous791677632
176970099469700995CT25GENICpossibly homozygous791677633
176970127169701272CT16GENIChomozygous791677634
176970155369701554GA22GENIChomozygous791677635
176970243469702435CA18GENICheterozygous791677636
176970294369702944TC9GENIChomozygous791677637
176970333869703339GT12GENIChomozygous791677638
176970353769703538GT53GENICheterozygous791677639
176970450469704505GA13GENIChomozygous791677640
176970917969709180TC16GENIChomozygous791677641
176971133369711334TG19GENIChomozygous791677642