chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1224799875224799876GA11GENIChomozygous108556108
1224799980224799981CT28GENIChomozygous108556109
1224800715224800716TC12GENIChomozygous108556110
1224800787224800788AT19GENIChomozygous108556111
1224800822224800823AG23GENIChomozygous108556112
1224802865224802866AC23GENIChomozygous108556113
1224802941224802942GA4GENIChomozygous108556114
1224803012224803013AG10GENIChomozygous108556115
1224803653224803654GA14GENIChomozygous108556116
1224804283224804284AG24GENIChomozygous108556117
1224804734224804735CT6GENIChomozygous108556118
1224804742224804743TC10GENIChomozygous108556119
1224804855224804856GA28GENIChomozygous108556120
1224804947224804948TC15GENIChomozygous108556121
1224804956224804957AG18GENIChomozygous108556122
1224805036224805037GA22GENIChomozygous108556123
1224806630224806631AG25GENIChomozygous108556124
1224807316224807317AG9GENIChomozygous108556125
1224807398224807399AG19GENIChomozygous108556126
1224807538224807539AG11GENIChomozygous108556127
1224807658224807659CT27GENIChomozygous108556128
1224807927224807928AG17GENIChomozygous108556129
1224808100224808101GA17GENIChomozygous108556130
1224808179224808180TC16GENIChomozygous108556131
1224808379224808380GA11GENIChomozygous108556132
1224808525224808526AT13GENIChomozygous108556133
1224808552224808553AC12GENIChomozygous108556134
1224808576224808577AG11GENIChomozygous108556135
1224809769224809770TA18GENIChomozygous108556136
1224809954224809955CT15GENIChomozygous108556137
1224810556224810557GA12GENIChomozygous108556138
1224810585224810586CT17GENIChomozygous108556139
1224810639224810640TC19GENIChomozygous108556140
1224811479224811480CG9GENIChomozygous108556146
1224811954224811955GC15GENIChomozygous108556147
1224812005224812006AG8GENIChomozygous108556148
1224812951224812952GA15GENIChomozygous108556149
1224814968224814969CT17GENIChomozygous108556150
1224815896224815897CT20GENIChomozygous108556151
1224817859224817860CT16GENIChomozygous108556152
1224818259224818260CT19GENIChomozygous108556153