chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141005837210058373AG27GENIChomozygous998301796
141005839310058394AC30GENIChomozygous998301797
141005854510058546CA33GENIChomozygous998301798
141005858910058590CT33GENIChomozygous998301799
141005869510058696CT31GENIChomozygous998301800
141005889610058897GA37GENIChomozygous998301801
141005934910059350GA18GENIChomozygous998301802
141006074310060744CT18GENIChomozygous998301803
141006082010060821AG13GENIChomozygous998301804
141006096610060967CT16GENIChomozygous998301805
141006108710061088GC20GENIChomozygous998301806
141006114010061141CT22GENIChomozygous998301807
141006114210061143AT21GENIChomozygous998301808
141006115310061154TC21GENIChomozygous998301809
141006119810061199GA18GENIChomozygous998301810
141006141410061415AC29GENIChomozygous998301811
141006142010061421GA27GENIChomozygous998301812
141006142310061424TA25GENIChomozygous998301813
141006144610061447CA18GENIChomozygous998301814
141006157910061580AG26GENIChomozygous998301815
141006158510061586AG24GENIChomozygous998301816
141006159510061596GA23GENIChomozygous998301817
141006163110061632CT27GENIChomozygous998301818
141006168610061687TC31GENIChomozygous998301819
141006169310061694AG34GENIChomozygous998301820
141006169410061695AG34GENIChomozygous998301821
141006170010061701CT34GENIChomozygous998301822
141006187310061874GA22GENIChomozygous998301823
141006187510061876CA22GENIChomozygous998301824