chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1228737670228737671AG55GENIChomozygous507216591
1228738748228738749AT57GENIChomozygous510482765
1228741237228741238TG49GENICpossibly homozygous510482766
1228741239228741240TG49GENICheterozygous510482767
1228741329228741330AAGAGAG27GENIChomozygous685167452
1228741505228741506A-34GENIChomozygous685167453
1228741525228741526A-31GENIChomozygous685167454
1228743096228743097AC45GENICheterozygous510482768
1228744220228744221TC66GENIChomozygous510482769
1228744463228744464CA66GENICpossibly homozygous510482770
1228744907228744908CT48GENICpossibly homozygous510482771
1228745221228745222TC48GENIChomozygous510482772
1228745396228745397TC43GENIChomozygous510482773
1228745721228745722AG49GENIChomozygous510482774
1228746722228746723TC41GENIChomozygous510482775
1228749142228749143GA52GENIChomozygous510482776
1228750707228750708G-1GENIChomozygous685167455
1228751658228751659CT48GENIChomozygous510482777
1228751732228751733CCATTT11GENIChomozygous685167456
1228751914228751915CT44GENIChomozygous510482778
1228752487228752488AG36GENIChomozygous510482779
1228753035228753036CCCACA4GENIChomozygous685167457
1228753085228753089ACAC----8GENICheterozygous685167458
1228753087228753089AC--8GENICheterozygous685167459
1228754285228754286CCT17GENICpossibly homozygous685167460
1228755467228755468GGCA14GENIChomozygous685167461
1228755483228755484AACACAC12GENICheterozygous685167462
1228755484228755485TC18GENICheterozygous510482780
1228755486228755487CCACA10GENICheterozygous685167465
1228755487228755488T-10GENICheterozygous685167464
1228755487228755488TTACAC8GENICpossibly homozygous685167467
1228756439228756440CCT6GENICheterozygous685167468
1228756440228756441T-6GENICheterozygous685167469
1228758692228758693CT51GENIChomozygous510482781
1228758718228758719AG48GENIChomozygous510482782