chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
132690341926903420GA50GENIChomozygous781903444
132690455026904551TG62GENIChomozygous781903445
132690487426904875TC58GENIChomozygous781903446
132690502526905026TC71GENIChomozygous781903447
132690579726905798AG50GENIChomozygous781903448
132690646326906464AC46GENIChomozygous781903449
132690772226907723CT59GENIChomozygous781903450
132690799526907996CT59GENIChomozygous781903451
132690806426908065TC60GENICpossibly homozygous781903452
132690829026908291GA55GENIChomozygous781903453
132690871226908713TC48GENIChomozygous781903454
132690888826908889CG61GENIChomozygous781903455
132690930926909310CT32GENIChomozygous781903456
132691026926910270GC68GENIChomozygous781903457
132691093226910933GT45GENIChomozygous781903458
132691109026911091GA44GENIChomozygous781903459
132691133226911333GA62GENIChomozygous781903460
132691164826911649CT69GENICpossibly homozygous781903461
132691245026912451TG62GENIChomozygous781903462
132691366226913663GA56GENIChomozygous781903463
132691717726917178CT75GENIChomozygous781903464
132691867226918673CT59GENIChomozygous781903465
132691996826919969AG90GENICpossibly homozygous781903466
132692003926920040AG92GENIChomozygous781903467
132692122326921224CT61GENIChomozygous781903468
132692176126921762TC44GENIChomozygous781903469
132692232326922324GA75GENIChomozygous781903470
132692238526922386AT82GENICpossibly homozygous781903471
132692256126922562TC70GENIChomozygous781903472
132692257626922577CA62GENIChomozygous781903473
132692271526922716AC50GENIChomozygous781903474
132692276726922768AG53GENIChomozygous781903475