chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3123227818123227819T74GENIChomozygous127925580
3123227827123227827G74GENIChomozygous127925581
3123227843123227843A76GENIChomozygous127925582
3123227849123227849CTCGTGG70GENIChomozygous127925583
3123227888123227889G62GENIChomozygous127925584
3123228027123228028C44GENIChomozygous130283029
3123229497123229502AGAAA13GENIChomozygous130283030
3123229503123229504GT13GENIChomozygous130290705
3123229488123229489AT20GENIChomozygous130290701
3123229490123229491AT18GENIChomozygous130290702
3123229492123229493AT17GENIChomozygous130290703
3123229494123229495AT14GENIChomozygous130290704
3123229505123229508AAA13GENIChomozygous130283031
3123229510123229512AA12GENIChomozygous130283032
3123229514123229515AT12GENIChomozygous130290706
3123229516123229517AT9GENIChomozygous130290707
3123229518123229520AA8GENIChomozygous130283033
3123229521123229522CT14GENIChomozygous130290708
3123236411123236412C43GENIChomozygous127925589
3123236421123236422G39GENIChomozygous127925590