chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101115721011157211TC41GENIChomozygous116734262
101115733911157340AG33GENIChomozygous116734263
101115860911158610GA31GENIChomozygous116858849
101115935711159358CT33GENIChomozygous116734264
101115937411159375CT22GENIChomozygous116734265
101116020811160209TC46GENIChomozygous116734269
101115981711159818CT28GENIChomozygous116734266
101116005611160057TC32GENIChomozygous116734267
101116006611160067GA26GENIChomozygous116734268
101116053411160535AG23GENICpossibly homozygous116734270
101116064311160644GA28GENIChomozygous116734271
101116102211161023AG34GENIChomozygous116734272
101116163911161640CT28GENIChomozygous116734273
101116214011162141AG22GENICpossibly homozygous116734274
101116219411162195CA33GENIChomozygous116734275
101116249011162491GA28GENIChomozygous116734276
101116314611163147TC22GENICpossibly homozygous116734277
101116351411163515TC26GENIChomozygous116734278
101116369811163699CA28GENIChomozygous116734279
101116420911164210CT29GENIChomozygous116734280
101116422911164230GA27GENIChomozygous116734281
101116509811165099AG34GENIChomozygous116734282
101116510211165103GA36GENIChomozygous116734283
101116522411165225TC32GENIChomozygous116734284
101116575811165759AC20GENIChomozygous116734285
101116693111166932TC19GENIChomozygous116734286
101116714111167142TG25GENIChomozygous116734287
101116802311168024GT38GENIChomozygous116734288
101116972811169729TC35GENIChomozygous116734289
101117041911170420TC37GENIChomozygous116734290
101117106911171070GC33GENIChomozygous116734291
101117135311171354CT23GENIChomozygous116734292
101117283511172836CT39GENICpossibly homozygous116734293
101117323411173235TC23GENIChomozygous116494294
101117349811173499GA27GENIChomozygous116734294
101117376511173766CG20GENIChomozygous116494296
101117387711173878TC23GENIChomozygous116494298
101117652211176523TA17GENIChomozygous116494302