chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8107544064107544065CT43GENIChomozygous138410176
8107544259107544260TC36GENIChomozygous138410177
8107544298107544299TC37GENIChomozygous138410178
8107544382107544383CG35GENIChomozygous138410179
8107547522107547523GA32GENIChomozygous138410180
8107547788107547789AG31GENIChomozygous138410181
8107548172107548173CA31GENICpossibly homozygous154540724
8107548172107548173CG31GENICheterozygous154540725