chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1221505421221505422AG16GENIChomozygous108994963
1221505840221505841GT22GENIChomozygous108994964
1221506459221506460CG22GENIChomozygous108994965
1221506554221506554CAAA15GENIChomozygous130833281
1221506852221506853TC29GENIChomozygous108994966
1221507010221507011AC16GENIChomozygous108994967
1221507481221507482CT19GENIChomozygous108994968
1221507574221507575CG12GENIChomozygous108994969
1221508175221508176GA2GENIChomozygous132008558
1221508443221508444GA2GENIChomozygous109538020
1221508686221508687GA2GENIChomozygous108544597
1221508711221508712AG2GENIChomozygous108770207
1221510995221510996TC22GENICheterozygous108544599
1221511070221511071AG3GENIChomozygous129860451
1221511077221511078GA2GENIChomozygous132273952
1221511301221511302AG4GENIChomozygous108994970
1221511313221511314AG5GENIChomozygous131796561
1221511400221511401TC8GENICheterozygous127578156
1221511582221511583TC2GENIChomozygous108994972
1221511583221511584GA2GENIChomozygous132008568
1221511587221511588AG2GENIChomozygous131796563
1221511641221511642AG5GENIChomozygous108544601
1221511724221511725TC4GENIChomozygous131796565
1221511755221511756TC4GENICheterozygous109569644
1221513725221513726AT16GENIChomozygous108994974
1221514248221514249TC12GENIChomozygous108994975
1221514419221514419T24GENIChomozygous130833282
1221514430221514431TC25GENIChomozygous108994976
1221514706221514707CT8GENIChomozygous108994977
1221515084221515085CT13GENIChomozygous109368439
1221515469221515469TTTCCCTTT11GENIChomozygous130833283
1221511499221511500GA3GENIChomozygous134511114
1221510699221510700TC2GENIChomozygous134511113