chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7145146563145146564TC26GENICpossibly homozygous118362286
7145147728145147729CA30GENICpossibly homozygous118362287
7145148101145148102AG21GENIChomozygous118362288
7145148126145148127AG24GENIChomozygous118362289
7145148400145148401TC25GENIChomozygous116378457
7145149929145149930GA32GENIChomozygous118362290
7145149955145149956TC26GENIChomozygous118362291
7145150310145150311CA20GENIChomozygous118362292
7145150986145150987TC31GENIChomozygous115946618
7145151089145151090GC21GENICpossibly homozygous118516072
7145151090145151091CT19GENIChomozygous118516073
7145151136145151137TC9GENIChomozygous118362293
7145151315145151316GC19GENICpossibly homozygous118362294
7145151424145151425GC29GENIChomozygous118362295
7145152460145152461TC26GENICpossibly homozygous118362296
7145152860145152861GC20GENICpossibly homozygous118362297
7145153663145153664AG18GENIChomozygous118362298
7145151185145151186TC21GENIChomozygous115946620