chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X2844912728449127T14GENIChomozygous129730850
X2844959728449598AT10GENIChomozygous125102807
X2845039428450395AG4GENIChomozygous125102808
X2845083028450831TC24GENIChomozygous119912654
X2845119428451195C5GENIChomozygous129730851
X2845968028459681AG3GENIChomozygous108248889
X2846053228460533GA27GENIChomozygous108248893
X2846108528461086AG21GENIChomozygous108248895
X2845990928459910CT28GENIChomozygous108377939
X2846012728460128GT23GENIChomozygous108377941
X2846294228462943GA16GENIChomozygous108377943
X2846351728463518CT29GENIChomozygous108377945
X2846437628464377CT36GENIChomozygous108377947
X2846453428464535GA18GENIChomozygous108248909
X2846522528465226TC31GENIChomozygous108248913
X2846556028465561AG23GENIChomozygous108248915
X2846556528465566AG21GENIChomozygous108248917
X2846616128466162AG7GENICheterozygous120104649
X2846814428468144ATCC31GENIChomozygous129730855
X2846450028464501A15GENIChomozygous131239748
X2846602628466027AT6GENICheterozygous133931285
X2846635228466353GA3GENICheterozygous133931286
X2846607228466073A5GENICheterozygous133929018
X2846832128468322TG21GENIChomozygous108441600