chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101115721011157211TC25GENIChomozygous116734262
101115733911157340AG30GENIChomozygous116734263
101115859111158592CT24GENIChomozygous117074830
101115860911158610GA20GENIChomozygous116858849
101116020811160209TC30GENIChomozygous116734269
101115981711159818CT36GENIChomozygous116734266
101116005611160057TC36GENIChomozygous116734267
101116006611160067GA37GENIChomozygous116734268
101116053411160535AG23GENIChomozygous116734270
101116064311160644GA23GENIChomozygous116734271
101116102211161023AG31GENIChomozygous116734272
101116163911161640CT22GENIChomozygous116734273
101116214011162141AG28GENIChomozygous116734274
101116219411162195CA20GENIChomozygous116734275
101116249011162491GA26GENIChomozygous116734276
101116314611163147TC21GENIChomozygous116734277
101116351411163515TC21GENIChomozygous116734278
101116369811163699CA17GENIChomozygous116734279
101116420911164210CT19GENIChomozygous116734280
101116422911164230GA21GENIChomozygous116734281
101116509811165099AG30GENIChomozygous116734282
101116510211165103GA28GENIChomozygous116734283
101116522411165225TC33GENIChomozygous116734284
101116575811165759AC25GENIChomozygous116734285
101116693111166932TC18GENIChomozygous116734286
101116714111167142TG24GENIChomozygous116734287
101116802311168024GT44GENIChomozygous116734288
101116972811169729TC15GENIChomozygous116734289
101117041911170420TC18GENIChomozygous116734290
101117106911171070GC34GENIChomozygous116734291
101117135311171354CT26GENIChomozygous116734292
101117283511172836CT25GENIChomozygous116734293
101117349811173499GA27GENIChomozygous116734294
101117323411173235TC17GENIChomozygous116494294
101117376511173766CG19GENIChomozygous116494296
101117387711173878TC26GENIChomozygous116494298
101117652211176523TA12GENIChomozygous116494302