chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X113965834113965835GC11GENIChomozygous108311493
X113970546113970547CA11GENIChomozygous108311508
X113970547113970548TC11GENIChomozygous108311510
X113977068113977069TC10GENIChomozygous108311516
X114018608114018609GT7GENIChomozygous108311568
X114018732114018733AG11GENIChomozygous108311570
X114018866114018867AT7GENIChomozygous108311572
X114018867114018868TG7GENIChomozygous108311574
X114019075114019076TA17GENIChomozygous108311576
X114019115114019116AC8GENIChomozygous108311578
X114019272114019273TC17GENIChomozygous108311580
X114019563114019564CT10GENIChomozygous108311584
X114024861114024862TG5GENIChomozygous108311592
X114024867114024868GT2GENIChomozygous108311594
X114018448114018449GA10GENIChomozygous108419302
X114018459114018460TC10GENIChomozygous108419304
X114028942114028943TC16GENIChomozygous108311614
X114028943114028944CT16GENIChomozygous108311616
X114095555114095556AC11GENICheterozygous108745363