chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
142293282322932824GA22GENIChomozygous786839946
142293447722934478TC18GENIChomozygous786839947
142293448022934481AC19GENIChomozygous786839948
142293451722934518TC23GENIChomozygous786839949
142293764622937647TA15GENIChomozygous786839950
142293947022939471CT7GENIChomozygous786839951
142294094922940950AG32GENIChomozygous786839952
142294134322941344CA30GENIChomozygous786839953
142294277722942778CA22GENIChomozygous786839954
142294389522943896AG37GENIChomozygous786839955
142294402922944030TA30GENIChomozygous786839956
142294751922947520CA19GENIChomozygous786839957
142294752122947522AC19GENIChomozygous786839958
142294826322948264CA18GENIChomozygous786839959
142294884322948844GA21GENIChomozygous786839960
142295235922952360CG18GENIChomozygous786839961
142295489422954895GA34GENICheterozygous786839962
142295552222955523CT28GENIChomozygous786839963
142295557922955580GT29GENIChomozygous786839964