chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4140887210140887211TG30GENIChomozygous969486338
4140887405140887406GC32GENIChomozygous969486339
4140887526140887527AG21GENIChomozygous969486340
4140892114140892115TA30GENIChomozygous969486341
4140894149140894150GA39GENIChomozygous969486342
4140894483140894484TC34GENIChomozygous969486343
4140896988140896989GA49GENIChomozygous969486344
4140899328140899329GA23GENIChomozygous969486345
4140902715140902716TC19GENIChomozygous969486346
4140902957140902958AG44GENIChomozygous969486347
4140903807140903808CT23GENIChomozygous969486348
4140906395140906396AG32GENIChomozygous969486349
4140908274140908275TG35GENIChomozygous969486350
4140908994140908995GC23GENIChomozygous969486351
4140909042140909043GA19GENIChomozygous969486352
4140909059140909060CA21GENIChomozygous969486353
4140909109140909110GA19GENIChomozygous969486354
4140909129140909130CT16GENIChomozygous969486355
4140909170140909171GA21GENIChomozygous969486356
4140909196140909197CT28GENIChomozygous969486357
4140909286140909287GC31GENIChomozygous969486358
4140913522140913523CT15GENIChomozygous969486359
4140916630140916631TG31GENIChomozygous969486360
4140916631140916632CA31GENIChomozygous969486361
4140916937140916938GA34GENIChomozygous969486362