chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
185827145758271458TC30GENIChomozygous110814037
185827250558272506GA28GENIChomozygous110814039
185827592258275923GT24GENIChomozygous110814041
185827855758278558CT27GENIChomozygous110814043
185828453858284539AC27GENIChomozygous110545485
185828492158284922AG22GENIChomozygous110814045
185828550958285510AT54GENIChomozygous110814047
185828651458286515AG21GENIChomozygous110475809
185827488958274890GA23GENIChomozygous119568741
185828614358286144AG35GENIChomozygous110475807
185828725958287260GA39GENICpossibly homozygous110814049
185828743258287433CT25GENIChomozygous110814051
185828745158287452CT30GENIChomozygous110814053
185828896658288967CT40GENICpossibly homozygous110814055
185828973858289739GA24GENIChomozygous110814057
185829005658290057GC28GENIChomozygous110814059
185829079558290796CT33GENIChomozygous110656471
185829111558291116TC31GENIChomozygous110656472
185829122258291223GA25GENIChomozygous110656473
185829136658291367CT39GENIChomozygous110656474
185829142058291421AG42GENIChomozygous110475816
185829154758291548GA29GENIChomozygous110814061
185829157058291571AG23GENIChomozygous110656475
185829436458294365AG30GENIChomozygous110475830
185829471658294717TC28GENIChomozygous110475839
185829487058294871GA27GENIChomozygous110814063
185830013058300131CA45GENIChomozygous110475869
185830030958300310TC31GENIChomozygous110475870