chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4136454775136454776GC30GENIChomozygous520073480
4136455016136455017CT40GENIChomozygous520073481
4136455211136455212CT50GENIChomozygous520073482
4136455928136455929CCG48GENIChomozygous690569217
4136460283136460284CT32GENIChomozygous520073483
4136460450136460451GA11GENIChomozygous520073484
4136461234136461235TC29GENICpossibly homozygous520073485
4136464169136464170CCA44GENIChomozygous690569218
4136468054136468055TC48GENIChomozygous520073486
4136469697136469698GT38GENIChomozygous520073487
4136471761136471762TC51GENIChomozygous520073488
4136473209136473210CT26GENIChomozygous523411563
4136473779136473780T-41GENIChomozygous690569219
4136474109136474110AG32GENIChomozygous520073489