chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6125042349125042350AT40GENIChomozygous794262825
6125043149125043150GT36GENIChomozygous794262826
6125045107125045108CT48GENICpossibly homozygous794262827
6125048772125048773GA48GENIChomozygous794262828
6125049812125049813TC43GENIChomozygous794262829
6125051702125051703TC59GENIChomozygous794262830
6125051787125051788GA62GENIChomozygous794262831
6125052367125052368TC43GENIChomozygous794262832
6125052674125052675CT50GENIChomozygous794262833
6125052929125052930CT39GENIChomozygous794262834
6125053620125053621AG51GENIChomozygous794262835
6125054104125054105CT65GENIChomozygous794262836
6125058255125058256GA47GENICpossibly homozygous794262837
6125061110125061111GT35GENIChomozygous794262838
6125066295125066296TC57GENIChomozygous794262839
6125067010125067011AC45GENIChomozygous794262840
6125067226125067227GA20GENICheterozygous794262841
6125067234125067235AG20GENICheterozygous794262842
6125067238125067239AG23GENICheterozygous794262843
6125067989125067990CT60GENIChomozygous794262844
6125068238125068239CT46GENICpossibly homozygous794262845
6125069020125069021TC51GENIChomozygous794262846
6125069192125069193CG43GENIChomozygous794262847
6125070462125070463GA61GENIChomozygous794262848
6125070954125070955CT50GENIChomozygous794262849
6125072010125072011GC48GENIChomozygous794262850
6125073846125073847CT54GENIChomozygous794262851
6125075490125075491GA37GENIChomozygous794262852
6125077163125077164TA42GENIChomozygous794262853
6125077737125077738GA32GENIChomozygous794262854
6125078090125078091AG25GENIChomozygous794262855
6125081226125081227AC60GENIChomozygous794262856