chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
173166177331661774TG50GENIChomozygous140099557
173166267031662670T31GENIChomozygous140019214
173166307631663077A41GENIChomozygous140019215
173166325531663256CG40GENIChomozygous140099558
173166466031664661CT44GENIChomozygous140099559
173166511731665118GA35GENIChomozygous140099560
173166544031665441CT47GENIChomozygous140099561
173166573631665736T52GENIChomozygous140019216
173166618831666189AG52GENIChomozygous140099562
173166743631667441CTTCC34GENIChomozygous140019217
173166778331667784TC49GENIChomozygous140099563
173166790631667907GA43GENIChomozygous140099564
173166857831668579GA48GENIChomozygous140099565
173166933831669339TC54GENIChomozygous140099566
173167231731672318CA51GENIChomozygous140099567
173167420431674205CT52GENIChomozygous140099568
173167509831675099GC30GENIChomozygous140099569
173167513231675138GAGAAG25GENICheterozygous140019218
173167509831675099G31GENICheterozygous403666483
173167513731675138G25GENICheterozygous403666484
173166297231662973CA12GENIChomozygous403666481
173166297231662973C12GENICheterozygous403666482
173167513731675138GA25GENICheterozygous403666485
173167517731675177A22GENIChomozygous140019219
173167542231675423TA39GENIChomozygous140099570
173167558031675580A43GENIChomozygous140019220
173167558131675582GT48GENIChomozygous140099571
173167570231675703GA45GENIChomozygous140099572
173167591031675911TA43GENIChomozygous140099573
173167611131676112AG50GENIChomozygous140099574
173167612631676127A47GENIChomozygous140019221
173167620331676204CT58GENIChomozygous140099575
173167632431676325CT50GENIChomozygous140099576
173167633231676333AG50GENIChomozygous140099577
173167649931676500GA56GENIChomozygous140099578
173167687331676873C30GENIChomozygous140019222
173167797731677978CT47GENIChomozygous140099579
173167835731678358GA46GENIChomozygous140099580
173167836031678361CT45GENIChomozygous140099581