chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
132690341926903420GA35GENIChomozygous980131350
132690455026904551TG25GENIChomozygous980131351
132690487426904875TC46GENIChomozygous980131352
132690502526905026TC30GENIChomozygous980131353
132690579726905798AG16GENIChomozygous980131354
132690772226907723CT26GENIChomozygous980131355
132690799526907996CT31GENIChomozygous980131356
132690806426908065TC42GENIChomozygous980131357
132690829026908291GA21GENIChomozygous980131358
132690871226908713TC32GENIChomozygous980131359
132690888826908889CG46GENIChomozygous980131360
132690930926909310CT33GENIChomozygous980131361
132691026926910270GC20GENIChomozygous980131362
132691093226910933GT30GENIChomozygous980131363
132691109026911091GA20GENIChomozygous980131364
132691133226911333GA26GENIChomozygous980131365
132691164826911649CT19GENIChomozygous980131366
132691245026912451TG38GENIChomozygous980131367
132691366226913663GA38GENIChomozygous980131368
132691717726917178CT9GENIChomozygous980131369
132691867226918673CT13GENIChomozygous980131370
132691996826919969AG12GENIChomozygous980131371
132692003926920040AG16GENIChomozygous980131372
132692122326921224CT20GENIChomozygous980131373
132692176126921762TC31GENIChomozygous980131374
132692232326922324GA19GENIChomozygous980131375
132692238526922386AT27GENIChomozygous980131376
132692256126922562TC11GENIChomozygous980131377
132692257626922577CA10GENIChomozygous980131378
132692271526922716AC19GENIChomozygous980131379
132692276726922768AG28GENICpossibly homozygous980131380