chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7128876648128876649CT62GENIChomozygous138221289
7128876953128876953G62GENIChomozygous145611528
7128876990128876991CT46GENIChomozygous145640304
7128877162128877163GA38GENIChomozygous145640305
7128877251128877252GA43GENIChomozygous145640306
7128877355128877356TC44GENIChomozygous145640307
7128878284128878285GA37GENIChomozygous145640308
7128878314128878315TA37GENIChomozygous138221290
7128879631128879632TC45GENIChomozygous138221294
7128879800128879801CT43GENIChomozygous138221295
7128881035128881036GA46GENIChomozygous145640309
7128881479128881480AG46GENIChomozygous138221296
7128877282128877282T43GENICpossibly homozygous137982924
7128879167128879167G44GENIChomozygous137982925
7128884347128884348AG36GENIChomozygous138221303
7128885637128885638AG43GENIChomozygous138221304
7128888078128888079CG48GENIChomozygous145640310
7128888150128888151CG45GENIChomozygous145640311
7128888231128888232GA49GENIChomozygous138221305
7128889389128889390TC53GENIChomozygous138221306
7128890023128890024AG45GENIChomozygous138221310
7128890024128890025GA45GENIChomozygous145640312
7128890243128890244TC45GENIChomozygous138221311
7128890416128890417TC38GENIChomozygous138221312
7128892534128892535CT35GENIChomozygous145640313
7128892575128892576TG42GENICpossibly homozygous145640314
7128896783128896784GA12GENIChomozygous138221314
7128893502128893503GA50GENIChomozygous145640315
7128893761128893762TC46GENIChomozygous145640316
7128895919128895920GA20GENIChomozygous145640317
7128896024128896025GA35GENIChomozygous145640318
7128896783128896784G12GENICheterozygous403226747