chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7145146563145146564TC20GENIChomozygous997511278
7145147728145147729CA21GENIChomozygous997511279
7145148101145148102AG25GENIChomozygous997511280
7145148126145148127AG26GENIChomozygous997511281
7145148400145148401TC28GENIChomozygous997511282
7145149929145149930GA25GENIChomozygous997511283
7145149955145149956TC27GENIChomozygous997511284
7145150310145150311CA27GENIChomozygous997511285
7145150986145150987TC31GENIChomozygous997511286
7145151089145151090GC20GENIChomozygous997511287
7145151090145151091CT21GENIChomozygous997511288
7145151136145151137TC31GENIChomozygous997511289
7145151185145151186TC27GENIChomozygous997511290
7145151315145151316GC25GENIChomozygous997511291
7145151424145151425GC12GENIChomozygous997511292
7145152460145152461TC16GENIChomozygous997511293
7145152860145152861GC27GENIChomozygous997511294
7145153663145153664AG5GENIChomozygous997511295