chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1157464291157464292CT16GENIChomozygous109154225
1157464806157464807AG15GENIChomozygous109154227
1157464909157464910AT20GENIChomozygous109154229
1157466126157466127CT7GENIChomozygous109154231
1157466179157466180AG5GENIChomozygous125430748
1157467372157467373AG10GENIChomozygous125403148
1157468241157468242TC21GENIChomozygous108325728
1157468748157468749TC19GENIChomozygous109154233
1157470447157470448CT27GENIChomozygous109154235
1157471671157471672AC21GENIChomozygous108325730
1157473671157473672GT37GENIChomozygous108325732
1157475917157475918CT8GENIChomozygous109154239
1157476224157476225CT12GENIChomozygous109154241
1157476752157476753TC5GENICheterozygous109154243
1157476927157476928CT3GENICheterozygous125430749
1157478188157478189AC22GENIChomozygous109154245
1157479204157479205AG23GENIChomozygous109154247
1157479392157479393GA17GENIChomozygous109154249
1157483555157483556CT8GENIChomozygous109154251
1157487440157487441TG15GENIChomozygous109154253
1157488567157488568GA17GENIChomozygous109154255
1157490939157490940AG23GENIChomozygous109154257
1157491443157491444CT30GENIChomozygous109154259
1157491880157491881TC17GENIChomozygous109154261