chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4136454775136454776GC12GENIChomozygous581830186
4136455016136455017CT38GENIChomozygous581830187
4136455211136455212CT31GENIChomozygous581830188
4136455928136455929CCG31GENIChomozygous719384442
4136460450136460451GA5GENIChomozygous581830189
4136461234136461235TC51GENIChomozygous581830190
4136462014136462015AT20GENIChomozygous581830191
4136463389136463390CA25GENIChomozygous581830192
4136463552136463553A-7GENIChomozygous719384443
4136463755136463757GG--4GENIChomozygous719384444
4136464504136464505AT19GENIChomozygous581830193
4136464843136464844AG29GENIChomozygous581830194
4136468054136468055TC20GENIChomozygous581830195
4136468193136468194AG44GENIChomozygous581830196
4136469697136469698GT40GENIChomozygous581830197
4136470136136470149ACCCCAATTGTAT-------------18GENIChomozygous719384445
4136470415136470416CT30GENIChomozygous581830198
4136471761136471762TC18GENIChomozygous581830199
4136473286136473304GTTATATACGTTTCCCTG------------------51GENIChomozygous719384446
4136473779136473780T-35GENICpossibly homozygous719384447
4136474109136474110AG49GENIChomozygous581830200