chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
123275550732755508TC24GENIChomozygous115310072
123275666732756668CA24GENIChomozygous115310074
123275672632756727AC20GENIChomozygous115310076
123275721532757216GA30GENIChomozygous115310078
123275744532757446AT29GENIChomozygous115310080
123275808032758081AG10GENIChomozygous115310082
123275891532758916CT20GENIChomozygous115310084
123276080532760806CT15GENIChomozygous115310086
123276164632761647GT24GENIChomozygous115310088
123276189932761900TC20GENIChomozygous115310090
123276266832762669TG6GENICheterozygous115310092
123276266832762669TG6GENICheterozygous115310092
123276266832762669TC3GENICheterozygous126221822
123276266832762669TC3GENICheterozygous126221823
123276269232762693GA18GENIChomozygous115310094
123276322732763228GT22GENIChomozygous115310096
123276326732763268CT27GENIChomozygous115310098
123276368432763685TA12GENIChomozygous115310100
123276460232764603AG27GENIChomozygous115310102
123276470632764707AG21GENIChomozygous115310104
123276501932765020AG18GENIChomozygous115310106
123276503432765035TC13GENIChomozygous115310108
123276513632765137GC23GENIChomozygous115310110
123276529832765299TC24GENICpossibly homozygous115310112
123276685532766856CT32GENIChomozygous115310114
123276731832767319TC16GENIChomozygous115310116
123276765832767659AG18GENIChomozygous115310118
123276773332767734TC20GENIChomozygous115310120
123276849732768498CG15GENIChomozygous115310122
123276886432768865AG14GENIChomozygous115310124
123276926832769269AG18GENIChomozygous115310126
123276927732769278CT14GENIChomozygous115310128
123276944732769448TA27GENIChomozygous115310130
123276983032769831TC18GENIChomozygous115310132
123277072832770729TC24GENIChomozygous115310134
123277110532771106TC10GENIChomozygous115310136
123277129832771299GA16GENIChomozygous115310138
123277154332771544TC13GENIChomozygous115424460
123277208932772090AG12GENIChomozygous115310140