chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8113701224113701225A11GENICpossibly homozygous403250062
8113701224113701225AT11GENICheterozygous403250063
8113701226113701227A6GENICheterozygous403250064
8113701226113701227AT6GENICheterozygous403250065
8113701228113701229A11GENICheterozygous403250066
8113701228113701229AT11GENICheterozygous403250067
8113703045113703046AT20GENIChomozygous154544153
8113703045113703046A20GENICheterozygous403250068
8113713648113713649AT41GENICpossibly homozygous138421375
8113727122113727123AC42GENIChomozygous138421376
8113729148113729149GA24GENIChomozygous138421377
8113729797113729798GA38GENIChomozygous138421378
8113729853113729854TC48GENIChomozygous138421379
8113729869113729870TC52GENIChomozygous138421380
8113769169113769170CG5GENIChomozygous142103542
8113782415113782416G23GENICheterozygous403250069
8113782417113782418GC23GENICheterozygous403250073
8113782415113782416GC23GENICheterozygous403250070
8113782415113782416GT23GENICheterozygous403250071
8113782417113782418G23GENICheterozygous403250072
8113782417113782418GT23GENICheterozygous403250074
8113782419113782420G23GENICheterozygous403250075
8113782419113782420GC23GENICheterozygous403250076
8113782421113782422G23GENICheterozygous403250077
8113782421113782422GC23GENICheterozygous403250078
8113782423113782424G23GENICheterozygous403250079
8113782423113782424GC23GENICheterozygous403250080
8113782425113782426G23GENICheterozygous403250081
8113782425113782426GC23GENICheterozygous403250082
8113799907113799908CT45GENIChomozygous138421381
8113805811113805812GT50GENICheterozygous142103543
8113805821113805822GT54GENICheterozygous142103544
8113805823113805824AG53GENICheterozygous142103545
8113829815113829816AT43GENICpossibly homozygous138421382
8113847491113847492GC46GENIChomozygous138421383
8113853778113853779CT42GENIChomozygous138421384
8113729898113729899T50GENIChomozygous138265951
8113741838113741839T42GENIChomozygous138265953