chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108968639689686397GA18GENIChomozygous116902921
108968746889687469AT23GENIChomozygous116820861
108968753289687533AG15GENIChomozygous116820865
108968815489688155AG26GENIChomozygous116820869
108968863589688636TC28GENIChomozygous116820871
108968933789689338TC13GENIChomozygous116902923
108968944289689443TC27GENIChomozygous116820873
108968954189689542GA23GENIChomozygous116902925
108969031789690318AG21GENIChomozygous116820875
108969069489690695TC13GENIChomozygous118069524
108969122789691228CT15GENIChomozygous116902927
108969244689692447AC18GENIChomozygous116902929
108969264489692645GA14GENIChomozygous116820879
108969436089694361AT14GENIChomozygous116982537
108969458189694582TC27GENIChomozygous116820891
108969492789694928GA23GENIChomozygous116902931
108969543589695436AT16GENIChomozygous116902933
108969547589695476CG23GENIChomozygous116902934
108969572689695727CT16GENIChomozygous116902936
108969584189695842AG15GENIChomozygous116902938
108969585689695857TC16GENIChomozygous116820893
108969633489696335AG29GENIChomozygous116902940
108969641289696413AG21GENIChomozygous116820895
108969704589697046CT11GENIChomozygous116902942
108969725789697258GA20GENIChomozygous116820897
108969748489697485TC18GENIChomozygous116902944
108969936089699361AG6GENIChomozygous116675738
108969936989699370CG4GENIChomozygous116675740
108969937189699372CG4GENIChomozygous116675742
108969429289694293AG18GENICpossibly homozygous117328708