chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
132690341926903420GA11GENIChomozygous976835089
132690455026904551TG27GENIChomozygous976835090
132690487426904875TC31GENIChomozygous976835091
132690502526905026TC30GENIChomozygous976835092
132690579726905798AG18GENIChomozygous976835093
132690643326906434GA25GENIChomozygous976835094
132690646326906464AC33GENIChomozygous976835095
132690772226907723CT14GENIChomozygous976835096
132690799526907996CT27GENIChomozygous976835097
132690806426908065TC23GENIChomozygous976835098
132690829026908291GA28GENIChomozygous976835099
132690871226908713TC20GENIChomozygous976835100
132690888826908889CG23GENIChomozygous976835101
132690930926909310CT20GENIChomozygous976835102
132691026926910270GC39GENIChomozygous976835103
132691093226910933GT19GENIChomozygous976835104
132691109026911091GA28GENIChomozygous976835105
132691133226911333GA35GENIChomozygous976835106
132691164826911649CT34GENIChomozygous976835107
132691245026912451TG26GENIChomozygous976835108
132691366226913663GA28GENIChomozygous976835109
132691717726917178CT26GENIChomozygous976835110
132691867226918673CT44GENIChomozygous976835111
132691996826919969AG33GENIChomozygous976835112
132692003926920040AG36GENIChomozygous976835113
132692122326921224CT31GENIChomozygous976835114
132692176126921762TC27GENIChomozygous976835115
132692232326922324GA32GENIChomozygous976835116
132692238526922386AT37GENIChomozygous976835117
132692256126922562TC41GENIChomozygous976835118
132692257626922577CA39GENIChomozygous976835119
132692271526922716AC27GENIChomozygous976835120
132692276726922768AG24GENIChomozygous976835121