chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1256806534256806535CG17GENICpossibly homozygous61170125
1256806581256806582TC23GENICpossibly homozygous61170126
1256807468256807469AG23GENICpossibly homozygous61170127
1256807866256807867CT13GENIChomozygous61170128
1256808595256808596GA13GENICpossibly homozygous61170129
1256810969256810971TC--1GENIChomozygous62277158
1256810973256810974AAGAGAT2GENICheterozygous62277159
1256811389256811390AC17GENICpossibly homozygous61170132
1256811439256811440CT2GENIChomozygous61170133
1256811780256811781A-12GENIChomozygous61170134
1256812113256812114CCATATTAA3GENIChomozygous61170135
1256812275256812276TC7GENIChomozygous61170136
1256812419256812420GT4GENIChomozygous61170137
1256812553256812554GA13GENIChomozygous61170138
1256812638256812639C-6GENICheterozygous62277160
1256812640256812643CAT---6GENICheterozygous62277161
1256812847256812848GA1GENIChomozygous61170140
1256813113256813114CA21GENICpossibly homozygous61170141
1256813409256813410AG9GENIChomozygous61170142