chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1228737670228737671AG19GENICpossibly homozygous589689348
1228738748228738749AT12GENIChomozygous591625079
1228738907228738908CT10GENICpossibly homozygous591625080
1228741329228741330AAGAGAG3GENIChomozygous723293539
1228741505228741506A-3GENICheterozygous723293540
1228741525228741526A-4GENIChomozygous723293541
1228744220228744221TC5GENICheterozygous591625081
1228744463228744464CA4GENICheterozygous591625082
1228744907228744908CT16GENICpossibly homozygous591625083
1228745221228745222TC10GENIChomozygous591625084
1228745396228745397TC6GENIChomozygous591625085
1228745721228745722AG4GENIChomozygous591625086
1228746722228746723TC5GENIChomozygous591625087
1228749142228749143GA14GENIChomozygous591625088
1228751658228751659CT5GENIChomozygous591625089
1228751914228751915CT4GENIChomozygous591625090
1228752487228752488AG5GENICheterozygous591625091
1228758718228758719AG6GENICheterozygous591625092