chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3176477651176477652TG40GENIChomozygous112218952
3176478083176478084AG42GENIChomozygous112218953
3176478986176478987GA34GENIChomozygous112218954
3176479436176479437AT30GENIChomozygous112218955
3176479522176479523CT34GENIChomozygous112218956
3176479741176479742CT44GENIChomozygous112218957
3176481310176481311CT36GENIChomozygous112218958
3176481701176481702CT42GENIChomozygous112218959
3176482102176482103AT46GENIChomozygous112218960
3176482144176482145CT42GENIChomozygous112218961
3176482173176482174AG46GENIChomozygous112218962
3176482773176482774GA20GENIChomozygous112218963
3176482958176482959AG25GENIChomozygous112218964
3176483753176483754TC20GENIChomozygous111841402
3176485235176485236TC23GENIChomozygous112218965
3176485663176485664AC20GENICpossibly homozygous119686719
3176485664176485665CA20GENICpossibly homozygous112319245
3176485991176485992TG13GENIChomozygous112218966
3176486757176486758GA28GENIChomozygous112218967
3176487969176487970TC29GENIChomozygous112218968
3176488663176488664TC46GENIChomozygous111841406