chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
159363552193635522AG19GENIChomozygous113177456
159363590893635909TA15GENIChomozygous113177458
159363605993636060AT20GENIChomozygous113177460
159363606793636068TG21GENIChomozygous113177462
159363617193636172GA22GENIChomozygous113177464
159363617893636179GA20GENIChomozygous113177466
159363619293636193CT17GENIChomozygous113177468
159363644693636447GA12GENIChomozygous113177470
159363682393636824CT29GENIChomozygous113177472
159363707493637075TC17GENIChomozygous112959352
159363805993638060TC26GENIChomozygous112959356
159363934493639345AG20GENIChomozygous112959360
159363990893639909CA16GENIChomozygous112959362
159364088093640881AG20GENIChomozygous112589940
159364105993641060CT19GENIChomozygous113177474
159363778893637789CT19GENIChomozygous113067134
159363855193638552GA15GENICpossibly homozygous113067136