chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X2236964122369642CG24GENIChomozygous883921046
X2237031322370314AG21GENIChomozygous883921047
X2237266122372662CT8GENICheterozygous883921048
X2237587022375871TG13GENIChomozygous883921049
X2237657522376576TC22GENIChomozygous883921050
X2237756822377569TA7GENIChomozygous883921051
X2237867322378674CT17GENIChomozygous883921052
X2237881522378816CT22GENIChomozygous883921053
X2237961722379618TG29GENIChomozygous883921054
X2237982222379823TA11GENIChomozygous883921055
X2238001722380018CT16GENIChomozygous883921056
X2238011022380111AG25GENIChomozygous883921057
X2238015122380152GC9GENIChomozygous883921058
X2238087322380874TA21GENIChomozygous883921059
X2238141622381417CT15GENIChomozygous883921060
X2238148922381490CT19GENIChomozygous883921061
X2238229822382299AT13GENIChomozygous883921062
X2238265522382656TC8GENIChomozygous883921063
X2238347022383471AT7GENIChomozygous883921064
X2238435222384353GA7GENIChomozygous883921065
X2238436222384363AG11GENIChomozygous883921066
X2238472922384730TC21GENIChomozygous883921067
X2238493522384936CA5GENICheterozygous883921068
X2238493922384940CA3GENICheterozygous883921069
X2238521122385212AG20GENICpossibly homozygous883921070
X2238557922385580AG35GENIChomozygous883921071
X2238798522387986CT12GENIChomozygous883921072
X2238829822388299TC7GENIChomozygous883921073
X2238838722388388TA7GENIChomozygous883921074
X2238917122389172CT11GENIChomozygous883921075
X2238927322389274GA18GENIChomozygous883921076
X2239033722390338AG24GENIChomozygous883921077
X2239119622391197TC19GENIChomozygous883921078
X2239549822395499TC12GENICheterozygous883921079
X2239565622395657TC20GENIChomozygous883921080