chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1212230789212230790CA9GENIChomozygous125308161
1212232148212232149CA7GENIChomozygous108988325
1212232401212232402GT19GENIChomozygous108988326
1212232675212232676AG10GENIChomozygous108526233
1212235696212235697TC23GENIChomozygous108988330
1212236314212236315AG11GENIChomozygous108988332
1212237803212237804AG8GENICheterozygous125340961
1212238216212238217GA21GENIChomozygous108988335
1212239162212239163CT12GENIChomozygous125437523
1212241968212241969TA10GENIChomozygous120489745
1212234677212234678TC26GENIChomozygous120489742
1212240101212240102CT16GENIChomozygous120489743
1212241850212241851GA15GENIChomozygous120489744
1212243535212243536GA24GENIChomozygous120489746
1212243859212243860CT18GENIChomozygous120489747
1212244131212244132GA30GENIChomozygous120591365
1212245421212245422GC15GENIChomozygous108988338
1212247120212247121CT3GENICheterozygous125534674
1212248663212248664CT18GENIChomozygous120489749
1212248719212248720TC14GENIChomozygous108988344
1212254301212254302CT8GENIChomozygous120902454
1212255064212255065CG27GENIChomozygous125308163
1212255108212255109CT16GENIChomozygous125308164
1212255134212255135TG9GENIChomozygous125468893
1212255135212255136TC9GENIChomozygous125437524
1212255141212255142CT11GENIChomozygous125308165
1212255197212255198AC6GENIChomozygous125308167
1212255237212255238GC11GENIChomozygous125308168
1212255250212255251CA14GENIChomozygous125308169
1212255283212255284CA6GENICheterozygous120906867