chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
99448686694486867GC4GENIChomozygous52053563
99449066994490670CA10GENIChomozygous52053575
99449067294490674AA--11GENICpossibly homozygous52280668
99449105094491051AG18GENIChomozygous52053579
99449138294491383TC23GENIChomozygous52053583
99449204794492048GA26GENIChomozygous52280674
99449228194492282CA32GENIChomozygous52053589
99449249794492498GGCA19GENIChomozygous52053593
99449292194492923TT--13GENIChomozygous52053594
99449293894492939CCT2GENIChomozygous52053598
99449340894493409CT28GENIChomozygous53485454
99448962094489621GA19GENIChomozygous53485449
99449009894490099CT18GENIChomozygous53485450
99449109394491107ACACACACACACAC--------------17GENIChomozygous53485451
99449289594492909GTTTTTTTGGGGGT--------------16GENIChomozygous53485452
99449325994493260CT27GENICpossibly homozygous53485453
99449350294493506ACAC----15GENIChomozygous53485455
99449352294493523AG19GENIChomozygous52280680
99449403794494041ACAC----15GENICheterozygous53485456
99449479694494797AG16GENIChomozygous52053600
99449495794494965TGTGTGTG--------5GENIChomozygous53238413