chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
181614106416141065AG21GENIChomozygous110453135
181614119016141202ACATTCATGCTA11GENIChomozygous129518845
181614212316142124CT19GENIChomozygous110284365
181614237716142378AG9GENIChomozygous110284367
181614288516142886CT16GENIChomozygous110284369
181614369716143698TC11GENIChomozygous110453136
181614652616146527TA18GENIChomozygous110453137
181614875616148757CT17GENIChomozygous110284383
181615024016150241CG14GENIChomozygous110453140
181615277216152773TC15GENIChomozygous110453141
181615456116154562AT21GENIChomozygous110284403
181615501916155020TC15GENIChomozygous110284405
181615504316155044CT14GENIChomozygous110453142
181615623116156232GT14GENICpossibly homozygous110284407
181615752716157528AT24GENIChomozygous110453143
181615473516154743TTTCTTTT21GENIChomozygous131203209
181615784216157843CT15GENIChomozygous110453144
181615871616158717AG18GENIChomozygous110284413
181615904716159050ACC11GENIChomozygous131203210
181615935016159351T12GENIChomozygous129518852
181616091216160913GA8GENIChomozygous110453145
181616221016162211TC28GENIChomozygous110284429
181616330716163308TC16GENIChomozygous110284433
181616531716165318CT11GENIChomozygous110453146
181616623016166231GA22GENIChomozygous110453147
181616947316169474CT10GENIChomozygous110453148
181617013216170133CT14GENIChomozygous110453149
181617221916172220TC17GENIChomozygous110284448
181617304416173045GA6GENIChomozygous110453150
181617531116175312GA15GENIChomozygous110453151
181617552916175530GA12GENIChomozygous110284464
181617558316175584GA17GENIChomozygous110453152
181617858816178589CA23GENIChomozygous110284476
181618222416182225CT18GENIChomozygous110453153
181618413116184131ACACAGC16GENIChomozygous131203211
181618606816186069AT15GENIChomozygous125412807
181618681616186817GA11GENIChomozygous110453154