chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5126784622126784623AG20GENIChomozygous113998782
5126785192126785193TC36GENIChomozygous113998784
5126786891126786892GA22GENIChomozygous113998786
5126787730126787731GA16GENIChomozygous113998788
5126789564126789565TC20GENIChomozygous113998790
5126790951126790952GC26GENIChomozygous113998792
5126791002126791003GA27GENIChomozygous113998794
5126791180126791181GA36GENIChomozygous113998798
5126791328126791329CG22GENIChomozygous113998800
5126791452126791453CA19GENIChomozygous113998802
5126791554126791555CT24GENIChomozygous113998804
5126791590126791591GC23GENIChomozygous114648370
5126791653126791654AG23GENIChomozygous113998806
5126791673126791674GA22GENIChomozygous113998808
5126791722126791723CT29GENIChomozygous113998809
5126791737126791738CA28GENIChomozygous113998811
5126791807126791808CT24GENIChomozygous113998813
5126791821126791822CT23GENIChomozygous113998815
5126791872126791873CA30GENIChomozygous113998817
5126791888126791889CG29GENIChomozygous114137419
5126791890126791891GT30GENIChomozygous118845368
5126791891126791892CG30GENIChomozygous114137420
5126791900126791901GT30GENIChomozygous113998819
5126792521126792522TC33GENIChomozygous113998827
5126792661126792662AG20GENICpossibly homozygous113998829
5126793181126793182GA22GENIChomozygous113998831
5126794490126794491CT37GENIChomozygous113998833
5126796861126796862AT16GENIChomozygous113998835
5126798209126798210CA26GENIChomozygous113998839
5126798351126798352AG26GENIChomozygous113998841
5126798646126798647CT6GENIChomozygous113998843
5126798816126798817GA19GENIChomozygous113998845
5126799502126799503TC17GENIChomozygous113998847
5126800146126800147GA20GENIChomozygous113998849
5126800424126800425CT18GENIChomozygous113998851
5126801073126801074GA22GENIChomozygous113998853
5126802364126802365CA15GENIChomozygous113998855
5126802943126802944AG35GENIChomozygous113998857
5126803816126803817AG12GENIChomozygous113998859