chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1212230789212230790CA9GENIChomozygous894881097
1212232148212232149CA7GENIChomozygous894881098
1212232401212232402GT19GENIChomozygous894881099
1212232675212232676AG10GENIChomozygous894881100
1212234677212234678TC26GENIChomozygous894881101
1212235696212235697TC23GENIChomozygous894881102
1212236314212236315AG11GENIChomozygous894881103
1212237803212237804AG8GENICheterozygous894881104
1212238216212238217GA21GENIChomozygous894881105
1212239162212239163CT12GENIChomozygous894881106
1212240101212240102CT16GENIChomozygous894881107
1212241850212241851GA15GENIChomozygous894881108
1212241968212241969TA10GENIChomozygous894881109
1212243535212243536GA24GENIChomozygous894881110
1212243859212243860CT18GENIChomozygous894881111
1212244131212244132GA30GENIChomozygous894881112
1212245421212245422GC15GENIChomozygous894881113
1212247120212247121CT3GENICheterozygous894881114
1212248663212248664CT18GENIChomozygous894881115
1212248719212248720TC14GENIChomozygous894881116
1212254301212254302CT8GENIChomozygous894881117
1212255064212255065CG27GENIChomozygous894881118
1212255108212255109CT16GENIChomozygous894881119
1212255134212255135TG9GENIChomozygous894881120
1212255135212255136TC9GENIChomozygous894881121
1212255141212255142CT11GENIChomozygous894881122
1212255197212255198AC6GENIChomozygous894881123
1212255237212255238GC11GENIChomozygous894881124
1212255250212255251CA14GENIChomozygous894881125
1212255283212255284CA6GENICheterozygous894881126