chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104595266645952667AG27GENIChomozygous116772134
104595272045952721TC21GENIChomozygous116772136
104595281345952814TC13GENIChomozygous116772138
104595284345952844AG10GENIChomozygous116772140
104595289945952900CT14GENIChomozygous116772142
104595293345952934CT15GENIChomozygous116772144
104595294945952950CG19GENIChomozygous116772146
104595303145953032CG21GENIChomozygous116772148
104595319245953193CT13GENIChomozygous116772150
104595340245953403TC10GENIChomozygous117218242
104595340445953405TC10GENIChomozygous117218244
104595346445953465CA7GENIChomozygous116772152
104595349045953491TC8GENIChomozygous116772154
104595353745953538TA11GENIChomozygous116772156
104595376045953761TC23GENIChomozygous116584860
104595384245953843AT21GENIChomozygous116772158
104595404345954044GA14GENIChomozygous116772162
104595436545954366AG17GENIChomozygous116772164
104595442245954423TA14GENIChomozygous116772166
104595486445954865TG20GENIChomozygous116772178
104595508845955089CT7GENIChomozygous116772180
104595515145955152GT8GENIChomozygous116772182
104595572345955724CT18GENIChomozygous116772184
104595615245956153CT3GENIChomozygous117218246
104595652845956529GA18GENICpossibly homozygous116772186
104596068745960688GA31GENIChomozygous116877473