chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
185688794856887949AG32GENIChomozygous110544003
185688814956888150AG46GENICpossibly homozygous110544005
185688818656888187TA35GENICpossibly homozygous110544007
185689077656890777TA44GENIChomozygous110921359
185689080556890806GT40GENIChomozygous110363168
185689204356892044AG55GENIChomozygous110544011
185689230156892302GA33GENIChomozygous110544013
185689290256892903GA46GENIChomozygous110363172
185689359356893594GA36GENIChomozygous110655451
185689368756893688TC40GENIChomozygous110544015
185689418456894185AG54GENICpossibly homozygous110544017
185689563456895635GA46GENIChomozygous110544019
185689578256895783GA32GENIChomozygous110544021
185689590756895908GA42GENIChomozygous110544024
185689624256896243GT38GENIChomozygous110544026
185689625956896260AC43GENIChomozygous110544028
185689670956896710AT58GENIChomozygous110544030
185689683656896837TC55GENIChomozygous110363179
185689735056897351CG40GENIChomozygous110544032
185689800956898010TA39GENIChomozygous110544034
185689896956898970CT44GENIChomozygous110544036
185689949356899494GA53GENIChomozygous110544038
185689987356899874GT53GENICpossibly homozygous110544040
185690072556900726CT29GENIChomozygous110544042
185690276856902769TC69GENIChomozygous110363187
185690345556903456CT36GENIChomozygous110544046
185690421256904213AG65GENICpossibly homozygous110363189
185690453356904534TC48GENICpossibly homozygous110544048
185690496356904964AC37GENICpossibly homozygous110544050
185690579856905799GT43GENIChomozygous110544052
185689117756891178TG40GENIChomozygous110686501
185689647456896475CT25GENIChomozygous119562823
185690654256906543AT48GENICpossibly homozygous110544054
185690712556907126GA50GENICpossibly homozygous110544056
185690783856907839GA38GENICheterozygous119562824
185690910456909105GA38GENIChomozygous110363193
185690910856909109GA39GENIChomozygous110544058
185690919756909198TG40GENIChomozygous110544062