chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7145146563145146564TC36GENIChomozygous118362286
7145147728145147729CA54GENICpossibly homozygous118362287
7145148101145148102AG49GENIChomozygous118362288
7145148115145148115A46GENIChomozygous133174144
7145148126145148127AG47GENIChomozygous118362289
7145148400145148401TC53GENIChomozygous116378457
7145149510145149513CTC43GENICpossibly homozygous133174145
7145149929145149930GA59GENIChomozygous118362290
7145149955145149956TC53GENIChomozygous118362291
7145150310145150311CA53GENICpossibly homozygous118362292
7145151136145151137TC70GENIChomozygous118362293
7145151315145151316GC62GENIChomozygous118362294
7145151424145151425GC54GENIChomozygous118362295
7145151593145151593CTTGGCATCATCACC58GENIChomozygous133174146
7145152087145152088GC29GENIChomozygous126649068
7145152460145152461TC45GENIChomozygous118362296
7145152860145152861GC68GENIChomozygous118362297
7145153663145153664AG55GENIChomozygous118362298
7145151185145151186TC65GENIChomozygous115946620
7145150986145150987TC44GENIChomozygous115946618
7145151089145151090GC63GENIChomozygous118516072
7145151090145151091CT63GENIChomozygous118516073