chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
97967103679671037AG45GENIChomozygous117594052
97967276079672760TGTTC16GENIChomozygous128726900
97967366779673668AT25GENIChomozygous117809024
97967366979673670C25GENIChomozygous128726906
97967367679673678TA27GENIChomozygous128726907
97967368079673682CC27GENIChomozygous128726908
97967369179673691C31GENIChomozygous128726909
97967369679673696T31GENIChomozygous128726910
97967370879673708T29GENIChomozygous128726911
97967371679673716C31GENIChomozygous128726912
97972742879727429G21GENIChomozygous128726913
97972743179727432G22GENIChomozygous128726914
97972749779727498A9GENIChomozygous128726915
97972750279727503A9GENIChomozygous128726916
97972750879727509GA9GENIChomozygous117380750
97972751279727513TG9GENIChomozygous117380751
97972753879727539C8GENIChomozygous128726917
97972758579727585C16GENIChomozygous128726918
97972760279727603C16GENIChomozygous128726919
97972761679727617GT19GENIChomozygous123203952
97972761779727618TG19GENIChomozygous123203953
97972763279727633AT22GENIChomozygous123203954
97972763379727634TA22GENIChomozygous123203955
97972766579727665A19GENIChomozygous128726920
97972766779727668G17GENIChomozygous128726921
97972767579727676TA18GENIChomozygous123203960
97972767779727678C18GENIChomozygous128726922
97972769079727691GA20GENIChomozygous117594054
97972769179727692AG21GENIChomozygous123203962
97973668879736689C39GENIChomozygous128726923
97973669279736693C38GENIChomozygous128726924
97970517879705179CT41GENICheterozygous128774621
97974656079746561CA16GENICpossibly homozygous128774622