chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108968639689686397GA22GENIChomozygous116902921
108968746889687469AT33GENIChomozygous116820861
108968753289687533AG29GENIChomozygous116820865
108968815489688155AG32GENIChomozygous116820869
108968863589688636TC33GENIChomozygous116820871
108968872789688728A26GENICpossibly homozygous130394169
108968933789689338TC45GENICpossibly homozygous116902923
108968944289689443TC44GENIChomozygous116820873
108968954189689542GA32GENIChomozygous116902925
108969031789690318AG40GENIChomozygous116820875
108969066789690668T30GENICpossibly homozygous130394170
108969122789691228CT36GENIChomozygous116902927
108969244689692447AC41GENIChomozygous116902929
108969264489692645GA39GENIChomozygous116820879
108969458189694582TC40GENIChomozygous116820891
108969585689695857TC39GENIChomozygous116820893
108969492789694928GA47GENIChomozygous116902931
108969543589695436AT31GENIChomozygous116902933
108969547589695476CG22GENIChomozygous116902934
108969572689695727CT38GENIChomozygous116902936
108969584189695842AG41GENIChomozygous116902938
108969076689690767C37GENIChomozygous131469113
108969210589692105C21GENICpossibly homozygous131469114
108969430589694305AAAT32GENIChomozygous131469115
108969429289694293AG40GENIChomozygous117328708
108969436089694361AT47GENIChomozygous116982537
108969633489696335AG30GENIChomozygous116902940
108969641289696413AG29GENIChomozygous116820895
108969672689696727G15GENIChomozygous131469116
108969733589697335TA25GENIChomozygous131469117
108969867889698678AAAG37GENICpossibly homozygous131469118
108969983689699840GTGT33GENIChomozygous131469119
108969937189699372CG21GENIChomozygous116675742
108969704589697046CT14GENIChomozygous116902942
108969725789697258GA11GENIChomozygous116820897
108969748489697485TC24GENIChomozygous116902944
108969936089699361AG23GENIChomozygous116675738
108969936989699370CG22GENIChomozygous116675740