chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
9113876000113876001AT42GENIChomozygous117645575
9113877659113877660GA35GENIChomozygous117645576
9113881015113881016GC47GENICpossibly homozygous117645577
9113881745113881746GA47GENIChomozygous117645578
9113884169113884170AG45GENICheterozygous117645580
9113886651113886652TC28GENIChomozygous117645582
9113887624113887625AC58GENIChomozygous117645583
9113888014113888015CA39GENIChomozygous117645586
9113893459113893460CG15GENICpossibly homozygous117427471
9113896373113896374TC11GENIChomozygous117631323
9113898093113898094TC37GENIChomozygous117645588
9113898682113898683TC43GENIChomozygous117645589
9113899794113899795TC21GENIChomozygous117645590