chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7128875847128875848CT17GENIChomozygous138221288
7128876648128876649CT22GENIChomozygous138221289
7128878314128878315TA14GENIChomozygous138221290
7128878404128878405TA34GENIChomozygous138221291
7128878601128878602CT18GENIChomozygous138221292
7128878830128878831GA17GENIChomozygous138221293
7128879631128879632TC23GENIChomozygous138221294
7128879800128879801CT23GENIChomozygous138221295
7128881479128881480AG18GENIChomozygous138221296
7128881511128881512GA15GENIChomozygous138221297
7128882741128882742CT18GENIChomozygous138221298
7128882952128882953CT18GENIChomozygous138221299
7128883159128883160GA11GENIChomozygous138221300
7128883543128883544CT18GENIChomozygous138221301
7128883973128883974CT16GENIChomozygous138221302
7128884347128884348AG14GENIChomozygous138221303
7128885637128885638AG18GENIChomozygous138221304
7128888231128888232GA21GENIChomozygous138221305
7128889389128889390TC17GENIChomozygous138221306
7128889671128889672CA23GENICpossibly homozygous138221307
7128889936128889937AG13GENIChomozygous138221308
7128889975128889976GA19GENIChomozygous138221309
7128890023128890024AG24GENIChomozygous138221310
7128890243128890244TC24GENIChomozygous138221311
7128890416128890417TC20GENIChomozygous138221312
7128894632128894633GA21GENIChomozygous138221313
7128896783128896784GA7GENIChomozygous138221314
7128896783128896784G7GENICheterozygous403226747
7128881954128881955T14GENIChomozygous137982926
7128883074128883075T16GENIChomozygous137982927
7128877282128877282T18GENIChomozygous137982924
7128879167128879167G15GENIChomozygous137982925