chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
92999377729993778TG10GENIChomozygous117302643
92999888629998887AG31GENIChomozygous117302661
92999890629998907AC29GENIChomozygous117302662
92999908729999088CA21GENIChomozygous117302663
92999914529999146GA36GENIChomozygous117302664
92999914829999149GA34GENIChomozygous117302665
92999915129999152GA36GENIChomozygous117302666
92999915629999157GA39GENIChomozygous117302667
93002912330029124CT50GENIChomozygous117302761
93002925330029254CT24GENIChomozygous117302763
93002945330029454GA40GENIChomozygous117302764
93002953630029537CG36GENIChomozygous117302765
93002959830029599TG35GENICpossibly homozygous117302766
93002965030029651AG29GENIChomozygous117302767
93002992930029930AC13GENIChomozygous117302773
93002994030029941TC13GENIChomozygous117302774
93002994230029943GC13GENIChomozygous117302775
93003427130034272CT31GENIChomozygous117302785
93003437130034372GA28GENIChomozygous117491929
93003881830038819AG34GENIChomozygous117302838
93003882130038822GC33GENIChomozygous117302839
93003882730038828AG31GENIChomozygous117696133
93003882830038829AT32GENIChomozygous117696135
93003883930038840CA33GENIChomozygous117302840
93003886930038870GT11GENIChomozygous117696137
93003888130038882TC11GENIChomozygous117302841
93003918930039190GC59GENIChomozygous117302847
93003933130039332CT49GENICpossibly homozygous117302849
93003956030039561GT41GENIChomozygous117491935
93003962330039624GT40GENIChomozygous117302850
93003963130039632TC35GENIChomozygous117302851
93005062130050622GC29GENIChomozygous117302879
93005070930050710CT31GENIChomozygous117302880
93005072230050723CA31GENIChomozygous117302881
93005090730050908TC44GENIChomozygous117302882
93005109330051094GT27GENIChomozygous117302883
93005150130051502TA44GENICpossibly homozygous117302888
93005170630051707AC40GENIChomozygous117302889
93005198030051981TC36GENICpossibly homozygous117698335
93005867230058673AG45GENICheterozygous117818807