chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
47069036470690378ACACACATACACAG27GENIChomozygous128047224
47069038670690387AC24GENIChomozygous112701152
47069044170690442CG6GENICheterozygous128126958
47069044370690444CG6GENICheterozygous128126959
47069044570690446CG6GENICheterozygous128126960
47069044770690448CG6GENICheterozygous128126961
47069091470690915GA36GENIChomozygous112701154
47069125570691256GA38GENIChomozygous112701156
47069133770691338CA37GENIChomozygous112701158
47069133870691339CG37GENIChomozygous112701160
47069156170691562AG44GENIChomozygous112701162
47069170170691702CA51GENIChomozygous112701164
47069199870691999GA40GENIChomozygous112701166
47069249270692493GT39GENIChomozygous112701168
47069285670692857GA39GENIChomozygous112701170
47069363470693635CT42GENIChomozygous112701172
47069444870694449TA49GENIChomozygous112701174
47069477970694780AG38GENIChomozygous112701176