chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1173382079173382080G-26GENIChomozygous712830576
1173383699173383700GA55GENIChomozygous573087321
1173385367173385368GGAA16GENICheterozygous712830577
1173385367173385368GGAAAA16GENICheterozygous712830579
1173385639173385640CT42GENIChomozygous575213304
1173386136173386137CT29GENIChomozygous575213305
1173386712173386714GG--10GENIChomozygous712830580
1173387165173387166GGA28GENIChomozygous712830581
1173387215173387216AG27GENIChomozygous573087322
1173387512173387523GCCTGAGTCCT-----------29GENIChomozygous712830582
1173387579173387580GA33GENIChomozygous573087323
1173387762173387763CT23GENIChomozygous573087324
1173388254173388255GA8GENICpossibly homozygous573087325
1173388335173388336AC8GENIChomozygous573087326
1173388376173388377AAGAATGAATGAAT13GENIChomozygous712830583
1173388457173388458AG23GENIChomozygous573087327
1173388656173388657CCT25GENICpossibly homozygous712830586
1173389172173389173CT36GENIChomozygous573087328
1173389216173389217TC38GENIChomozygous573087329
1173389232173389233GA39GENIChomozygous573087330
1173389662173389663TC42GENIChomozygous573087331
1173389783173389784TA22GENIChomozygous573087332
1173389871173389872GA38GENIChomozygous573087333
1173390048173390049CG39GENIChomozygous573087334
1173390090173390091CT50GENIChomozygous573087335
1173390202173390203TC31GENIChomozygous573087336
1173390347173390348AG21GENIChomozygous575213306
1173390388173390389CCTGTG13GENIChomozygous712830587
1173390403173390404CT19GENIChomozygous573087337
1173390856173390857GA25GENIChomozygous573087338
1173390869173390870GC25GENIChomozygous573087339
1173391329173391330CA33GENIChomozygous573087340