chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108968639689686397GA44GENIChomozygous116902921
108968746889687469AT49GENIChomozygous116820861
108968753289687533AG31GENIChomozygous116820865
108968815489688155AG25GENIChomozygous116820869
108968863589688636TC44GENIChomozygous116820871
108968872789688728A46GENICpossibly homozygous130394169
108968933789689338TC61GENIChomozygous116902923
108968944289689443TC48GENIChomozygous116820873
108968954189689542GA50GENIChomozygous116902925
108969031789690318AG59GENIChomozygous116820875
108969066789690668T38GENICpossibly homozygous130394170
108969076689690767C47GENIChomozygous131469113
108969122789691228CT66GENIChomozygous116902927
108969210589692105C29GENICpossibly homozygous131469114
108969244689692447AC57GENIChomozygous116902929
108969264489692645GA46GENIChomozygous116820879
108969429289694293AG50GENIChomozygous117328708
108969430589694305AAAT40GENICpossibly homozygous131469115
108969458189694582TC59GENIChomozygous116820891
108969492789694928GA46GENIChomozygous116902931
108969543589695436AT47GENIChomozygous116902933
108969633489696335AG40GENIChomozygous116902940
108969547589695476CG39GENIChomozygous116902934
108969572689695727CT53GENIChomozygous116902936
108969584189695842AG39GENIChomozygous116902938
108969585689695857TC42GENIChomozygous116820893
108969436089694361AT52GENIChomozygous116982537
108969641289696413AG36GENIChomozygous116820895
108969672689696727G14GENIChomozygous131469116
108969704589697046CT41GENIChomozygous116902942
108969725789697258GA25GENIChomozygous116820897
108969733589697335TA32GENICpossibly homozygous131469117
108969748489697485TC35GENIChomozygous116902944
108969867889698678AAAG39GENIChomozygous131469118
108969983689699840GTGT65GENIChomozygous131469119
108969937189699372CG37GENIChomozygous116675742
108969936089699361AG41GENIChomozygous116675738
108969936989699370CG38GENIChomozygous116675740