chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1791034489103449CA69GENICpossibly homozygous145027199
1791037059103706AC50GENICpossibly homozygous140051140
1791044069104407CT41GENIChomozygous145027200
1791046089104609TC42GENIChomozygous145027201
1791046149104615CT42GENIChomozygous145027202
1791051789105179AG56GENIChomozygous140051141
1791053209105321AG56GENIChomozygous140051142
1791054939105494AG51GENIChomozygous145027203
1791073929107393CA47GENICpossibly homozygous145027204
1791074189107419AG53GENIChomozygous145027205
1791082659108266AG47GENIChomozygous140051143