chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
123275550732755508TC26GENIChomozygous115310072
123275666732756668CA28GENIChomozygous115310074
123275672632756727AC31GENICpossibly homozygous115310076
123275721532757216GA27GENICpossibly homozygous115310078
123275744532757446AT19GENIChomozygous115310080
123275808032758081AG28GENIChomozygous115310082
123275891532758916CT15GENIChomozygous115310084
123276080532760806CT13GENIChomozygous115310086
123276164632761647GT16GENICpossibly homozygous115310088
123276189932761900TC28GENIChomozygous115310090
123276266832762669TG17GENIChomozygous115310092
123276269232762693GA18GENIChomozygous115310094
123276322732763228GT23GENIChomozygous115310096
123276326732763268CT27GENIChomozygous115310098
123276368432763685TA12GENIChomozygous115310100
123276460232764603AG30GENIChomozygous115310102
123276470632764707AG19GENIChomozygous115310104
123276501932765020AG35GENIChomozygous115310106
123276503432765035TC35GENIChomozygous115310108
123276513632765137GC43GENIChomozygous115310110
123276529832765299TC27GENIChomozygous115310112
123276685532766856CT16GENIChomozygous115310114
123276731832767319TC19GENIChomozygous115310116
123276765832767659AG30GENIChomozygous115310118
123276773332767734TC26GENIChomozygous115310120
123276849732768498CG27GENIChomozygous115310122
123276886432768865AG25GENIChomozygous115310124
123276926832769269AG25GENIChomozygous115310126
123276927732769278CT28GENIChomozygous115310128
123276944732769448TA31GENIChomozygous115310130
123276983032769831TC20GENIChomozygous115310132
123277072832770729TC23GENIChomozygous115310134
123277110532771106TC33GENIChomozygous115310136
123277129832771299GA34GENIChomozygous115310138
123277154332771544TC29GENIChomozygous115424460
123277208932772090AG24GENIChomozygous115310140