chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
46217889462178895TC23GENIChomozygous56918064
46217890662178907TG26GENIChomozygous56918066
46217897062178971GA35GENIChomozygous56918067
46217962662179627GC13GENICheterozygous57835644
46217963862179639AG10GENICheterozygous56918069
46217973062179731CT3GENICheterozygous56918070
46218001762180018GGGT9GENIChomozygous56918071
46218058962180590TTA22GENICheterozygous56918072
46218146862181469AC24GENICheterozygous57330709
46218187162181872AATT1GENIChomozygous56918073
46218192962181930C-26GENIChomozygous56918074
46218193462181935CT30GENIChomozygous56918076
46218195462181955CCT25GENIChomozygous56918077
46218195962181960CT33GENICheterozygous57330711
46218196062181961CT33GENICheterozygous57330713
46218196462181965CT28GENICheterozygous57733350
46218196562181966CT30GENICpossibly homozygous57330715
46218210662182118TTGGTTGGTTGG------------3GENIChomozygous56918078
46218368962183690CCAGG24GENIChomozygous56918079
46218561862185619CCA20GENIChomozygous56918080
46218671262186713CT37GENIChomozygous56918081
46218756762187568G-17GENIChomozygous56918082
46219150162191502AATG38GENIChomozygous56918083
46219150962191510GGTA39GENICpossibly homozygous56918084
46219161762191621TGTG----11GENICpossibly homozygous56918085
46219563062195634TACA----22GENIChomozygous56918087
46219611662196117G-23GENIChomozygous56918088
46219694762196948AG49GENIChomozygous56918089
46220007462200075AC42GENIChomozygous56918090
46220075262200755TCT---3GENIChomozygous56918091
46220075562200756C-4GENIChomozygous56918092
46220075962200760TTC3GENIChomozygous56918093
46220076962200770CT6GENICheterozygous56918095
46220077262200773C-1GENIChomozygous56918096
46220079662200797T-4GENIChomozygous56918097
46220081062200813CTC---4GENIChomozygous56918098
46220082162200824TCC---5GENICheterozygous56918100
46220082862200829C-6GENIChomozygous56918101
46220083262200839CCTCCTC-------5GENIChomozygous56918102