chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4140887210140887211TG6GENIChomozygous984977273
4140887405140887406GC21GENIChomozygous984977274
4140887526140887527AG21GENIChomozygous984977275
4140894149140894150GA28GENIChomozygous984977276
4140894483140894484TC24GENIChomozygous984977277
4140894658140894659GC34GENIChomozygous984977278
4140896988140896989GA19GENIChomozygous984977279
4140899328140899329GA26GENIChomozygous984977280
4140901019140901020TC6GENIChomozygous984977281
4140902715140902716TC18GENIChomozygous984977282
4140902957140902958AG19GENIChomozygous984977283
4140903807140903808CT24GENIChomozygous984977284
4140906395140906396AG22GENIChomozygous984977285
4140908274140908275TG20GENIChomozygous984977286
4140908994140908995GC15GENIChomozygous984977287
4140909042140909043GA22GENIChomozygous984977288
4140909059140909060CA26GENIChomozygous984977289
4140909109140909110GA27GENIChomozygous984977290
4140909129140909130CT25GENIChomozygous984977291
4140909170140909171GA26GENIChomozygous984977292
4140909196140909197CT32GENIChomozygous984977293
4140909244140909245GT35GENIChomozygous984977294
4140909248140909249TA37GENIChomozygous984977295
4140909269140909270GA34GENIChomozygous984977296
4140909286140909287GC34GENIChomozygous984977297
4140916630140916631TG27GENIChomozygous984977298
4140916631140916632CA26GENIChomozygous984977299
4140916937140916938GA15GENIChomozygous984977300