chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141005837210058373AG33GENIChomozygous976942787
141005839310058394AC37GENIChomozygous976942788
141005854510058546CA39GENIChomozygous976942789
141005858910058590CT48GENIChomozygous976942790
141005869510058696CT22GENIChomozygous976942791
141005889610058897GA35GENIChomozygous976942792
141005934910059350GA27GENIChomozygous976942793
141006074310060744CT17GENIChomozygous976942794
141006082010060821AG11GENIChomozygous976942795
141006096610060967CT21GENIChomozygous976942796
141006108710061088GC24GENIChomozygous976942797
141006114010061141CT19GENIChomozygous976942798
141006114210061143AT18GENIChomozygous976942799
141006115310061154TC23GENIChomozygous976942800
141006119810061199GA36GENIChomozygous976942801
141006141410061415AC28GENICpossibly homozygous976942802
141006142010061421GA25GENIChomozygous976942803
141006142310061424TA22GENIChomozygous976942804
141006144610061447CA23GENIChomozygous976942805
141006157910061580AG25GENIChomozygous976942806
141006158510061586AG23GENIChomozygous976942807
141006159510061596GA23GENIChomozygous976942808
141006163110061632CT29GENIChomozygous976942809
141006168610061687TC37GENIChomozygous976942810
141006169310061694AG35GENIChomozygous976942811
141006169410061695AG35GENIChomozygous976942812
141006170010061701CT36GENIChomozygous976942813
141006187310061874GA19GENIChomozygous976942814
141006187510061876CA19GENIChomozygous976942815