chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
13205487032054871AG71GENICpossibly homozygous108067561
13205525532055256AG67GENIChomozygous108067562
13205575532055756CT60GENIChomozygous108067563
13205625732056258GA60GENIChomozygous108067564
13205631632056317GC71GENIChomozygous108067565
13205690032056901TC52GENIChomozygous108067566
13205834932058350TA70GENICpossibly homozygous108067567
13205860532058606GA72GENIChomozygous108067568
13205860832058608GC72GENIChomozygous127369998
13205874732058750GGC68GENIChomozygous127369999
13205969032059692AC44GENIChomozygous127370000
13205969432059697TTA45GENIChomozygous127370001
13206039932060400GA62GENIChomozygous108067569
13206064332060644CT66GENIChomozygous108067570
13206369932063700CT59GENIChomozygous108067571
13206434632064347TC54GENIChomozygous108067572
13206457732064578AC74GENIChomozygous108067573
13206538332065384AG69GENICpossibly homozygous108067574
13206577832065779AG80GENIChomozygous108067575
13206578032065781TC78GENIChomozygous108067576
13206591732065917CTCCCTCGC63GENIChomozygous130814787
13206594132065942CT66GENIChomozygous108838642
13206592632065927CT64GENIChomozygous108838641