chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
109073270990732710CT25GENIChomozygous116821053
109073275490732755AG25GENIChomozygous116904879
109073283290732833CA20GENIChomozygous116821055
109073369090733691AT13GENIChomozygous116821057
109073387590733876GA20GENIChomozygous116821059
109073389290733893CA24GENIChomozygous116821061
109073410290734103CA20GENIChomozygous116821063
109073482490734825TC18GENIChomozygous116821065
109073539690735397GA15GENIChomozygous116821069
109073576290735763CT22GENIChomozygous116821071
109073991890739919CT23GENIChomozygous117087901
109074003090740031TC17GENIChomozygous116821073
109074201990742020TC18GENIChomozygous116904887
109074297990742980TC11GENIChomozygous116821077
109074304090743041TG18GENICpossibly homozygous116904891
109074388490743885AG5GENIChomozygous116821079
109074407490744075CT19GENIChomozygous117087903
109074773890747739AT15GENIChomozygous117087905