chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
28646928886469289TA8GENIChomozygous971880920
28646934786469348AG10GENIChomozygous971880921
28647051386470514AG13GENIChomozygous971880922
28647175286471753GA19GENIChomozygous971880923
28647192886471929AG18GENIChomozygous971880924
28647227586472276CT10GENIChomozygous971880925
28647333786473338TC9GENIChomozygous971880926
28647447386474474AG12GENIChomozygous971880927
28647454386474544AC11GENIChomozygous971880928
28647528586475286TG10GENIChomozygous971880929
28647576086475761GA11GENIChomozygous971880930
28647606886476069CA20GENIChomozygous971880931
28647683786476838CG22GENIChomozygous971880932
28647733186477332TC11GENIChomozygous971880933
28647738386477384GT7GENIChomozygous971880934
28647976486479765TC11GENIChomozygous971880935
28648006586480066GA23GENIChomozygous971880936
28648100986481010CT17GENIChomozygous971880937
28648123686481237TG8GENICpossibly homozygous971880938
28648166386481664GA8GENIChomozygous971880939
28653152986531530AG6GENIChomozygous971880940
28653153986531540GA8GENIChomozygous971880941
28654686686546867GA5GENIChomozygous971880942
28655833186558332CT19GENIChomozygous971880943
28655886786558868CT23GENIChomozygous971880944