chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141005437210054373AC30INTERGENIChomozygous800215942
141005799910058000TC18INTERGENIChomozygous800215943
141005837210058373AG32INTERGENIChomozygous800215944
141005839310058394AC33INTERGENIChomozygous800215945
141005854510058546CA32INTERGENIChomozygous800215946
141005858910058590CT35INTERGENIChomozygous800215947
141005869510058696CT28INTERGENIChomozygous800215948
141005889610058897GA37INTERGENIChomozygous800215949
141005934910059350GA33INTERGENIChomozygous800215950
141006074310060744CT32GENIChomozygous800215951
141006082010060821AG48GENIChomozygous800215952
141006096610060967CT27GENIChomozygous800215953
141006108710061088GC36GENIChomozygous800215954
141006114010061141CT26GENIChomozygous800215955
141006114210061143AT26GENIChomozygous800215956
141006115310061154TC26GENIChomozygous800215957
141006119810061199GA28GENIChomozygous800215958
141006131410061315AG25GENICheterozygous800215959
141006141410061415AC17GENIChomozygous800215960
141006142010061421GA17GENIChomozygous800215961
141006142310061424TA18GENIChomozygous800215962
141006144610061447CA19GENIChomozygous800215963
141006157910061580AG36GENIChomozygous800215964
141006158510061586AG38GENIChomozygous800215965
141006159510061596GA37GENIChomozygous800215966
141006163110061632CT29GENIChomozygous800215967
141006168610061687TC18GENIChomozygous800215968
141006169310061694AG17GENIChomozygous800215969
141006169410061695AG17GENIChomozygous800215970
141006170010061701CT23GENIChomozygous800215971
141006187310061874GA29GENIChomozygous800215972
141006187510061876CA29GENIChomozygous800215973