chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
31843537818435379AG10GENIChomozygous112414613
31843544318435444GT12GENIChomozygous112414615
31843547718435478CT17GENICheterozygous112414617
31843553518435536AT29GENIChomozygous112414621
31843553818435539AC29GENIChomozygous111476936
31843554518435546CT34GENIChomozygous111476937
31843561918435620TG46GENICheterozygous111476941
31843565318435654GC45GENIChomozygous112414623
31843570018435701TC62GENIChomozygous111476944
31843573618435737GT54GENICheterozygous112414625
31843574218435743CA53GENICheterozygous111476945
31843577518435776CT47GENICheterozygous112414627
31843579318435794TG29GENICheterozygous112414629
31843580318435804AG22GENICheterozygous112414631
31843580618435807GT21GENICheterozygous111476947
31843581318435814AT25GENICheterozygous111476950
31843583518435836GA39GENICheterozygous112414633
31843585518435856CA41GENIChomozygous112414635
31843587718435878CA52GENICheterozygous112414637
31843596918435970TC49GENICheterozygous112414639
31843604218436043CG46GENIChomozygous111886999
31843620318436204GT39GENICheterozygous112414641
31843628118436282TC35GENICheterozygous112414643
31843628918436290TG36GENICheterozygous112414645
31843637118436372TC33GENICheterozygous112414647
31843640018436401AG36GENICheterozygous112414649
31843647418436475CA26GENICheterozygous112414651
31843648418436485AT22GENICheterozygous112414653
31843654118436542GA22GENICheterozygous112414655
31843665118436652GC19GENICheterozygous112414657
31843669918436700TC25GENIChomozygous112414659
31843670018436701GC24GENIChomozygous112414661
31843670718436708TA25GENICheterozygous112414663
31843672518436726TG34GENIChomozygous112414665