chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106613337766133378C-24GENIChomozygous51907758
106613475866134759CCTCTG18GENIChomozygous51479126
106613475966134760AT10GENIChomozygous51479127
106613476166134762CT20GENICheterozygous51479128
106613712666137127T-3GENIChomozygous51907760
106614093066140931CG6GENIChomozygous51479147
106614093166140932CA5GENIChomozygous51479148
106614093966140940GT7GENIChomozygous51479149
106614094166140942A-6GENIChomozygous51479150
106614095866140959GC10GENIChomozygous51479151
106614096066140961GT10GENIChomozygous51479152
106614096366140964GT10GENIChomozygous51479153
106614096666140967T-10GENIChomozygous51479154
106614098566140986AT7GENIChomozygous51479155
106614098766140988GA7GENIChomozygous51479156
106614099066140991A-7GENIChomozygous51479157
106614100066141001A-7GENIChomozygous51479158
106614101466141015A-7GENIChomozygous51479159
106614102866141029A-4GENIChomozygous51479160
106614104066141041TC3GENIChomozygous51479162
106614108966141090A-2GENIChomozygous51479168
106614110966141110CCA3GENIChomozygous51479169
106614119266141199CCCAGCC-------5GENIChomozygous51479170
106614150666141507GGA16GENICheterozygous51678674
106614704566147046G-22GENIChomozygous51479181
106614715766147158C-9GENIChomozygous51479182
106615071066150711CCAA15GENICheterozygous51479187
106615071066150711CCA15GENICheterozygous51479188
106615676866156769AG27GENIChomozygous51479193