chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
37971409379714094GT29GENICpossibly homozygous789038184
37971463479714635CA22GENIChomozygous789038185
37971551579715516AG29GENIChomozygous789038186
37971672479716725CT14GENIChomozygous789038187
37971794479717945GC47GENIChomozygous789038188