chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
154856523248565233GA30GENIChomozygous48303982
154856543748565438AG32GENIChomozygous48303983
154856565148565652TC17GENIChomozygous48303985
154856609248566093GA17GENIChomozygous48824101
154856652748566528GA20GENIChomozygous48824103
154856794648567947AG18GENIChomozygous48824105
154856795648567957TC19GENIChomozygous48824107
154856816048568161AG25GENIChomozygous48824110
154856922648569227TC11GENIChomozygous48824112
154856939148569392CT12GENIChomozygous48824114
154856974348569744TC23GENIChomozygous48824116
154857030848570309AG19GENIChomozygous48824118
154857041848570419TC24GENIChomozygous48824120
154857175048571752TT--12GENIChomozygous48824122
154857177148571772CT22GENICheterozygous48671713
154857296648572967GA18GENIChomozygous48824124
154857307148573072AG23GENIChomozygous48824126
154857325548573256GA33GENIChomozygous48824128
154857362748573628GA19GENICpossibly homozygous48824130
154857396748573968GA15GENIChomozygous48824132
154857445448574455GA26GENIChomozygous48824134
154857453048574531AG29GENICpossibly homozygous48824136
154857559148575592G-7GENIChomozygous48303986
154857562548575626C-11GENIChomozygous48303987
154857593548575936AC28GENIChomozygous48824138
154857598748575988AG27GENIChomozygous48824141
154857621448576215C-17GENIChomozygous48824143
154857621648576218AG--17GENIChomozygous48824145
154857625948576260GT18GENIChomozygous48824147
154857632048576321CCA23GENIChomozygous48824149
154857653248576533CT22GENIChomozygous48824151
154857675448576755GA22GENIChomozygous48824153
154857688348576884CT17GENIChomozygous48824155
154857833648578337GA23GENIChomozygous48824157
154857868848578689TA26GENICpossibly homozygous48824159
154857876148578762GC25GENIChomozygous48824161
154857900048579001CA30GENICheterozygous48824163
154857900048579001CCAAAA29GENICpossibly homozygous48824165
154857903148579032CG26GENIChomozygous48824167