chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
116693624366936244AT28GENIChomozygous115888470
116693672166936722CT22GENIChomozygous115888472
116693864866938649CT49GENIChomozygous115888474
116693880566938806CT31GENIChomozygous115888476
116693938666939387CT46GENIChomozygous115888478
116694138366941384AC15GENIChomozygous115888480
116694269566942696CT32GENIChomozygous115888482
116694290766942908TA51GENIChomozygous115888484
116694402666944027AT45GENIChomozygous115888486
116694663466946635AT24GENICheterozygous118162843
116694824466948245GA19GENIChomozygous115888490
116695125866951259AG43GENIChomozygous115888492
116695315366953154AG27GENIChomozygous115888494
116695323866953239GA32GENIChomozygous115888496
116695571166955712CT39GENIChomozygous115888498
116695588966955890AG59GENIChomozygous115888500
116695672766956728AG41GENIChomozygous115888502
116695694066956941TA32GENIChomozygous115888504
116695702966957030TC28GENIChomozygous115888506
116695799366957994TC40GENICpossibly homozygous116048042
116695968066959681TC63GENIChomozygous115888508
116695984966959850GA44GENIChomozygous115888510
116696069566960696CT24GENIChomozygous115888514
116696110466961105GT31GENIChomozygous115888518
116696128066961281GA67GENIChomozygous115888520