chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
135579115155791152GT19GENICpossibly homozygous668857276
135579166055791661CT20GENICpossibly homozygous668857277
135579214955792150GA21GENIChomozygous668857278
135579303055793031AG6GENIChomozygous668857279
135579307355793074T-6GENIChomozygous768271376
135579405955794060AAG5GENICheterozygous768271377
135579417355794174CA10GENIChomozygous668857280
135579501655795017CT13GENIChomozygous668857281
135579512755795128AG21GENIChomozygous668857282
135579548355795484TC14GENIChomozygous668857283
135579568655795687GGC11GENIChomozygous768271378
135579639955796400GA27GENICpossibly homozygous668857284
135579807855798079AACCCC2GENIChomozygous768271380
135579909955799100AC12GENICpossibly homozygous668857285
135579987755799878AG1GENIChomozygous668857286
135580011755800118AC2GENIChomozygous668857287
135580029855800299CT23GENICpossibly homozygous668857288
135580038555800386GA15GENICpossibly homozygous668857289
135580062355800624CG9GENIChomozygous668857290
135580131055801311GT6GENICheterozygous668857291
135580164955801650AG22GENICpossibly homozygous668857292