chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7145146563145146564TC48GENIChomozygous118362286
7145147728145147729CA52GENIChomozygous118362287
7145148101145148102AG65GENIChomozygous118362288
7145148115145148115A58GENIChomozygous133174144
7145148126145148127AG59GENIChomozygous118362289
7145148400145148401TC59GENIChomozygous116378457
7145149510145149513CTC56GENIChomozygous133174145
7145149929145149930GA51GENIChomozygous118362290
7145149955145149956TC59GENIChomozygous118362291
7145150310145150311CA63GENICpossibly homozygous118362292
7145150986145150987TC66GENIChomozygous115946618
7145151089145151090GC68GENIChomozygous118516072
7145151315145151316GC59GENIChomozygous118362294
7145151090145151091CT68GENIChomozygous118516073
7145151136145151137TC53GENIChomozygous118362293
7145151185145151186TC52GENIChomozygous115946620
7145151424145151425GC62GENIChomozygous118362295
7145151593145151593CTTGGCATCATCACC43GENIChomozygous133174146
7145152087145152088GC29GENIChomozygous126649068
7145152460145152461TC52GENIChomozygous118362296
7145152860145152861GC59GENIChomozygous118362297
7145153663145153664AG67GENIChomozygous118362298