chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
123275397232753973TC11GENIChomozygous115310070
123275550732755508TC27GENIChomozygous115310072
123275666732756668CA27GENIChomozygous115310074
123275672632756727AC34GENICpossibly homozygous115310076
123275721532757216GA51GENIChomozygous115310078
123275744532757446AT21GENIChomozygous115310080
123275808032758081AG30GENIChomozygous115310082
123275891532758916CT17GENIChomozygous115310084
123276080532760806CT35GENIChomozygous115310086
123276189932761900TC37GENIChomozygous115310090
123276266832762669TG48GENIChomozygous115310092
123276269232762693GA47GENIChomozygous115310094
123276322732763228GT28GENIChomozygous115310096
123276326732763268CT23GENIChomozygous115310098
123276368432763685TA20GENIChomozygous115310100
123276460232764603AG38GENIChomozygous115310102
123276470632764707AG39GENIChomozygous115310104
123276501932765020AG41GENIChomozygous115310106
123276503432765035TC37GENIChomozygous115310108
123276513632765137GC33GENIChomozygous115310110
123276529832765299TC31GENIChomozygous115310112
123276685532766856CT39GENIChomozygous115310114
123276731832767319TC28GENIChomozygous115310116
123276765832767659AG37GENIChomozygous115310118
123276773332767734TC37GENIChomozygous115310120
123276849732768498CG30GENIChomozygous115310122
123276886432768865AG29GENIChomozygous115310124
123276926832769269AG39GENIChomozygous115310126
123276927732769278CT35GENIChomozygous115310128
123276944732769448TA32GENIChomozygous115310130
123276983032769831TC21GENIChomozygous115310132
123277072832770729TC31GENIChomozygous115310134
123277110532771106TC34GENIChomozygous115310136
123277129832771299GA41GENIChomozygous115310138
123277154332771544TC40GENIChomozygous115424460
123277208932772090AG48GENIChomozygous115310140