chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
148160101881601019A-1GENIChomozygous745033470
148160147481601475TC22GENIChomozygous629520634
148160185981601860TA14GENICpossibly homozygous629520635
148160188881601889AG17GENIChomozygous629520636
148160192281601923GA19GENIChomozygous629520637
148160194181601942TC14GENIChomozygous629520638
148160231181602312TC21GENICpossibly homozygous629520639
148160247181602474CTC---13GENICpossibly homozygous745033471
148160275781602758AAT5GENICheterozygous745033472
148160278981602790AG11GENIChomozygous629520640
148160282181602822AG14GENICpossibly homozygous629520641
148160299981603000AG13GENIChomozygous629520642
148160318481603185GA11GENICpossibly homozygous629520643
148160353981603540CT11GENICpossibly homozygous629520644
148160362381603624GA21GENICpossibly homozygous629520645
148160386581603866CCCT2GENIChomozygous745033474
148160386881603869TC2GENIChomozygous629520646
148160416381604164CG13GENIChomozygous629520647
148160437181604372GT28GENIChomozygous629520648
148160462781604628AG19GENICpossibly homozygous629520649
148160469281604693AC8GENIChomozygous629520650
148160470481604705CT11GENIChomozygous629520651
148160486881604869GA17GENIChomozygous629520652
148160489481604895GA15GENICpossibly homozygous629520653
148160514481605145CG7GENIChomozygous629520654
148160569981605700TG14GENICpossibly homozygous629520655
148160607181606072TG17GENICpossibly homozygous629520656
148160611381606114TTTTG1GENIChomozygous745033475
148160611781606118GT1GENIChomozygous629520657
148160691181606912TC13GENICpossibly homozygous629520658
148160920981609210CT16GENICpossibly homozygous629520659
148160970281609703GA19GENICheterozygous629520660
148160972681609727TG7GENIChomozygous629520661
148161055381610554TC8GENICheterozygous629520662