chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1221505421221505422AG23GENIChomozygous108994963
1221505840221505841GT28GENIChomozygous108994964
1221506459221506460CG31GENIChomozygous108994965
1221506554221506554CAAA24GENIChomozygous130833281
1221506852221506853TC26GENIChomozygous108994966
1221507010221507011AC15GENIChomozygous108994967
1221507481221507482CT24GENIChomozygous108994968
1221507574221507575CG24GENIChomozygous108994969
1221507970221507971GA3GENICheterozygous134324676
1221508018221508019CG4GENICheterozygous134324677
1221508046221508047AT4GENICheterozygous134324678
1221508025221508026GA4GENICheterozygous132556319
1221508447221508448CT3GENICheterozygous134324679
1221508711221508712AG1GENIChomozygous108770207
1221508686221508687GA2GENICheterozygous108544597
1221511301221511302AG2GENIChomozygous108994970
1221511321221511322CT2GENIChomozygous109538021
1221513725221513726AT25GENIChomozygous108994974
1221514248221514249TC29GENIChomozygous108994975
1221514419221514419T29GENIChomozygous130833282
1221514430221514431TC33GENIChomozygous108994976
1221514706221514707CT22GENIChomozygous108994977
1221515084221515085CT20GENIChomozygous109368439
1221515469221515469TTTCCCTTT15GENIChomozygous130833283