chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103788883837888839TA31GENICheterozygous51851274
103788883937888840CT31GENICheterozygous51851276
103789175637891757AG14GENICheterozygous51851310
103790796537907966CT32GENICheterozygous51851400
103794529037945291AG21GENICheterozygous51420083
103794533237945333CT16GENICheterozygous51420084
103796779637967797TC11GENICheterozygous52140967
103799121837991219TC37GENICheterozygous51420187
103800367138003672GA17GENICheterozygous51420255
103802021138020212TTCAGG30GENICheterozygous51420342
103803560038035601TC34GENICheterozygous51420404
103804755938047560CT26GENICheterozygous52141085
103804765938047660CT31GENICheterozygous51420444
103804854538048546TC36GENICheterozygous51420448
103805646338056464TC16GENICheterozygous51420473
103805963838059639GA26GENICheterozygous52141121
103811160538111606GA35GENICheterozygous52141216
103811318638113187AAT56GENICheterozygous52141236
103811326538113266CT42GENICheterozygous52141238
103816885738168858AG33GENICheterozygous51420797
103818187938181880GGA17GENICheterozygous52141489
103819439438194395CT28GENICheterozygous52141528
103819446338194464CT55GENICheterozygous52141530
103819477338194774C-12GENICheterozygous52141532
103820731038207311GA35GENICheterozygous52141570
103821090638210907CA23GENICheterozygous51420872
103822914338229144CT14GENICheterozygous52141602
103822915938229160AC12GENICheterozygous51420904
103823072438230725TG39GENICheterozygous51420907
103823135738231358AG21GENICheterozygous52141614
103828251338282514TC21GENICheterozygous51420970
103829143438291435CG16GENICheterozygous52042202
103829640138296402AG10GENICheterozygous52042222