chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1228737670228737671AG29GENIChomozygous579049516
1228738748228738749AT22GENIChomozygous581169680
1228741329228741330AAGAGAG5GENIChomozygous716943523
1228741505228741506A-5GENIChomozygous716943524
1228741525228741526A-4GENIChomozygous716943525
1228744220228744221TC24GENICheterozygous581169681
1228744463228744464CA8GENICheterozygous581169682
1228744907228744908CT21GENIChomozygous581169683
1228745221228745222TC17GENIChomozygous581169684
1228745396228745397TC24GENICpossibly homozygous581169685
1228745721228745722AG5GENIChomozygous581169686
1228746722228746723TC20GENICheterozygous581169687
1228749142228749143GA22GENIChomozygous581169688
1228751658228751659CT10GENICpossibly homozygous581169689
1228751914228751915CT7GENIChomozygous581169690
1228752487228752488AG19GENICpossibly homozygous581169691
1228758692228758693CT19GENICpossibly homozygous581169692
1228758718228758719AG14GENICpossibly homozygous581169693