chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
47069038670690387AC13GENIChomozygous112701152
47069041070690412AC11GENIChomozygous132601988
47069078170690782CT34GENIChomozygous113032611
47069091470690915GA30GENIChomozygous112701154
47069125570691256GA36GENIChomozygous112701156
47069133770691338CA39GENIChomozygous112701158
47069133870691339CG38GENIChomozygous112701160
47069156170691562AG34GENIChomozygous112701162
47069170170691702CA37GENIChomozygous112701164
47069199870691999GA42GENICpossibly homozygous112701166
47069249270692493GT45GENIChomozygous112701168
47069285670692857GA39GENIChomozygous112701170
47069363470693635CT27GENIChomozygous112701172
47069372170693722AG27GENIChomozygous113032612
47069444870694449TA35GENIChomozygous112701174
47069477970694780AG36GENIChomozygous112701176