chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1219003121219003122GA66GENIChomozygous108540034
1219005311219005312TC57GENICpossibly homozygous108540036
1219006361219006362AG77GENIChomozygous108540038
1219007358219007359TC70GENIChomozygous108540040
1219008046219008047TC65GENIChomozygous108540042
1219010153219010154TC15GENIChomozygous108540044
1219010775219010776AG38GENIChomozygous108540046
1219012645219012646GA61GENIChomozygous108540048
1219013023219013024GA57GENICpossibly homozygous108540050
1219014181219014182AG35GENIChomozygous108540052
1219016898219016899CA78GENIChomozygous108540054
1219018057219018058GA59GENIChomozygous108540056
1219019565219019566AG47GENIChomozygous108540058
1219021331219021332GC51GENICheterozygous108540060
1219021335219021336GC54GENICheterozygous108540062
1219022013219022014GA52GENIChomozygous108540064
1219023133219023134GA46GENIChomozygous108540066
1219024812219024813GT19GENICpossibly homozygous108540068
1219026006219026007TC71GENIChomozygous108540070
1219026088219026089TC70GENIChomozygous108540072
1219026787219026788GA87GENICpossibly homozygous108540074
1219027538219027539CA77GENICpossibly homozygous108540076
1219031340219031341AG80GENIChomozygous108540078
1219031596219031597AC42GENICpossibly homozygous108540080
1219033095219033096GC49GENICpossibly homozygous108540082
1219036556219036557GA65GENIChomozygous108540084
1219037762219037763AC78GENICpossibly homozygous108540086
1219038065219038066AT45GENICpossibly homozygous108540088
1219040526219040527AG51GENIChomozygous108540090
1219040723219040724AG60GENIChomozygous108540092
1219042635219042636TG63GENIChomozygous108540094
1219045027219045028GA48GENICpossibly homozygous108540096
1219045378219045379CT72GENICpossibly homozygous108540098
1219045657219045658AG44GENIChomozygous108540100
1219049839219049840CT80GENIChomozygous108540102