chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1228737670228737671AG19GENIChomozygous815266592
1228738748228738749AT19GENIChomozygous815266593
1228741231228741232TTCG13GENIChomozygous815266594
1228741329228741330AAGAGAG16GENIChomozygous815266595
1228744220228744221TC14GENIChomozygous815266596
1228744463228744464CA17GENIChomozygous815266597
1228744907228744908CT13GENIChomozygous815266598
1228745221228745222TC14GENIChomozygous815266599
1228745396228745397TC19GENIChomozygous815266600
1228745721228745722AG7GENIChomozygous815266601
1228746722228746723TC13GENIChomozygous815266602
1228749142228749143GA20GENIChomozygous815266603
1228751658228751659CT23GENICpossibly homozygous815266604
1228751914228751915CT17GENIChomozygous815266605
1228752487228752488AG20GENIChomozygous815266606
1228755483228755484AACACAC12GENIChomozygous815266607
1228755486228755487CCACA12GENIChomozygous815266608
1228755487228755488TC12GENIChomozygous815266609
1228758692228758693CT15GENIChomozygous815266610
1228758718228758719AG15GENIChomozygous815266611