chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
89694022296940223TC16GENIChomozygous52745589
89694023596940236GA16GENICheterozygous52745590
89694181796941818CT11GENICheterozygous52745591
89694226196942262AT12GENIChomozygous52745592
89694279896942799TG12GENIChomozygous52745594
89694311096943111TTA21GENICheterozygous52745595
89694355996943560CT22GENICheterozygous52745596
89694381696943817CT15GENICheterozygous52745597
89694383096943831TG13GENICheterozygous53366559
89694385096943851TC12GENICheterozygous53366560
89694385596943856CT12GENICheterozygous52745598
89694385696943857AG12GENIChomozygous52745599
89694394096943941AAACAC9GENICheterozygous53366561
89694403296944038ATCCCC------11GENIChomozygous53404988
89694403996944040TTGGGG11GENIChomozygous53404989
89694415896944159AG7GENICheterozygous53366562
89694417896944179CT7GENICheterozygous53366563
89694431596944316AG10GENICheterozygous53366564
89694436896944369TC12GENICheterozygous54413224
89694638396946384AG13GENICheterozygous52745602
89694661196946612GA14GENICheterozygous53366565
89694667796946678CT8GENIChomozygous52745603
89694683496946835TC16GENICheterozygous53366566
89694846096948461TC11GENIChomozygous52745605
89695051496950515TG13GENICheterozygous53366567
89695105996951060GA10GENIChomozygous52745608
89695125796951258CT11GENIChomozygous52745609
89695216696952167GA8GENICheterozygous52745610
89695234296952343CCG12GENIChomozygous52745611
89695624596956246AC9GENICheterozygous52745615
89695640496956405T-19GENIChomozygous52745616
89695676096956761CT16GENICheterozygous53366571
89695684396956844A-11GENICheterozygous53366572
89695810296958103CG10GENICheterozygous53366574
89695838896958389CG14GENIChomozygous52745618
89695856496958565CT8GENICheterozygous53010449