chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104591030745910308CT38GENICpossibly homozygous52052944
104591066645910667TC37GENIChomozygous51443476
104591130845911309TTCC12GENICheterozygous51443479
104591141245911413CA20GENIChomozygous52052946
104591160245911604CA--7GENIChomozygous51443483
104591161345911614GGT10GENIChomozygous51443485
104591166545911666CT20GENICpossibly homozygous51443486
104591167745911678GA19GENIChomozygous51443487
104591168245911683CG21GENIChomozygous51443488
104591246645912467GA56GENIChomozygous52052948
104591293845912939TC26GENIChomozygous51443489
104591454645914547CA14GENICheterozygous52052950
104591455245914553TG15GENICheterozygous52052952
104591479545914796G-9GENIChomozygous51443496
104591487745914878CCT7GENICheterozygous51443497
104591491745914918T-4GENIChomozygous51443499
104591508445915085A-28GENICpossibly homozygous51443501
104591657645916577TC44GENIChomozygous51443502
104591792645917927TC35GENIChomozygous51443505
104591958045919581AC25GENIChomozygous51443507
104592039545920396GA33GENIChomozygous52052954
104592170145921702C-28GENICheterozygous51636535
104592171545921716G-30GENICheterozygous51443510
104592240845922409CA36GENIChomozygous52052957
104592403445924035AG35GENIChomozygous51443513
104592437845924379GA44GENIChomozygous52052959
104592561245925613GC32GENIChomozygous52052961
104592784345927844AG35GENIChomozygous51443518
104592812945928132CCT---34GENIChomozygous52052963