chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
91721733117217332CG14GENIChomozygous117682162
91721736417217365CT14GENIChomozygous117682164
91721770317217704AG8GENIChomozygous117682166
91721785517217856CT14GENIChomozygous117682168
91721785617217857AG14GENIChomozygous117682170
91721801717218018GT14GENIChomozygous117675166
91721903217219033AT4GENIChomozygous120294753
91721924417219245GA11GENIChomozygous117682172
91721934017219341GA19GENIChomozygous117270231
91721938417219385GA5GENIChomozygous117675170
91721942217219423GA10GENICheterozygous117270233
91721999617219997AC9GENIChomozygous117682174
91722015217220153CT15GENIChomozygous117270234
91722109117221092CG25GENIChomozygous117270235
91722114617221147TG21GENIChomozygous117270236
91722135617221357GA16GENIChomozygous117270237
91722141317221414GC10GENIChomozygous117270238