chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4145377793145377794CG44GENIChomozygous112870837
4145377958145377959CT55GENICpossibly homozygous112870838
4145378139145378140GC51GENIChomozygous112870839
4145380277145380278AG25GENIChomozygous112870841
4145380893145380894GA53GENIChomozygous112870842
4145381300145381301AG52GENIChomozygous112870843
4145381344145381345GA63GENIChomozygous112870844
4145382075145382076TC40GENIChomozygous112870845
4145382782145382782CACACT11GENICheterozygous128087979
4145379202145379207TTGTC59GENIChomozygous128087975
4145382526145382532TACACA25GENIChomozygous128087976
4145382588145382590AT27GENIChomozygous128087977
4145382703145382705CA9GENIChomozygous128087978
4145381839145381840CT17GENIChomozygous128136025
4145382822145382832CTCACACACT2GENIChomozygous128087980
4145385061145385062GA20GENIChomozygous112870846
4145385904145385905CT45GENIChomozygous112870848
4145386018145386022ACAC46GENIChomozygous128087984
4145383020145383032CACTCACACACA14GENIChomozygous128087981
4145383063145383063CA15GENIChomozygous128087982
4145384927145384927A23GENIChomozygous128087983
4145386110145386111GA49GENIChomozygous112870849
4145386529145386529CAAA34GENICpossibly homozygous128087985
4145386860145386861AC46GENIChomozygous112870851
4145387719145387720AG44GENIChomozygous112870852
4145388150145388151CT36GENIChomozygous112870855