chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X6889258368892584TC17GENIChomozygous810249114
X6889287668892877CT8GENIChomozygous810249115
X6889338168893382CG28GENIChomozygous810249116
X6889355068893551TC21GENIChomozygous810249117
X6889377368893774AG23GENIChomozygous810249118
X6889392368893924TC32GENIChomozygous810249119
X6889478168894782CG22GENIChomozygous810249120
X6889686468896865GA29GENIChomozygous810249121
X6889719468897195CA16GENIChomozygous810249122
X6889869768898698AC23GENIChomozygous810249123
X6889947268899473GA32GENIChomozygous810249124
X6890232468902325GA29GENIChomozygous810249125
X6890344568903446CT28GENICpossibly homozygous810249126