chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4140887405140887406GC22GENIChomozygous882967513
4140887526140887527AG9GENIChomozygous882967514
4140889290140889291CA12GENIChomozygous882967515
4140892114140892115TA26GENIChomozygous882967516
4140894149140894150GA16GENIChomozygous882967517
4140894483140894484TC10GENIChomozygous882967518
4140894658140894659GC25GENICpossibly homozygous882967519
4140896988140896989GA23GENIChomozygous882967520
4140899328140899329GA26GENIChomozygous882967521
4140903807140903808CT24GENIChomozygous882967522
4140904293140904294CG4GENIChomozygous882967523
4140907775140907776TG8GENICheterozygous882967524
4140908274140908275TG21GENIChomozygous882967525
4140908994140908995GC20GENIChomozygous882967526
4140909042140909043GA15GENIChomozygous882967527
4140909059140909060CA18GENIChomozygous882967528
4140909129140909130CT15GENIChomozygous882967529
4140909170140909171GA10GENIChomozygous882967530
4140909196140909197CT19GENIChomozygous882967531
4140909244140909245GT15GENIChomozygous882967532
4140909269140909270GA8GENIChomozygous882967533
4140909286140909287GC17GENIChomozygous882967534
4140913522140913523CT4GENIChomozygous882967535
4140916630140916631TG13GENIChomozygous882967536
4140916631140916632CA13GENIChomozygous882967537
4140916937140916938GA25GENIChomozygous882967538