chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4153874951153874952TC7GENIChomozygous112890487
4153875716153875717AC24GENIChomozygous112890488
4153875760153875761GA23GENIChomozygous112890489
4153876544153876545GA17GENIChomozygous112890490
4153876607153876608GA16GENIChomozygous112890491
4153877590153877591TC22GENIChomozygous112890492
4153878243153878244TC16GENIChomozygous112890493
4153878862153878863AG23GENIChomozygous112890494
4153879296153879297GC6GENIChomozygous112890495
4153885866153885867TC26GENIChomozygous112890496
4153889856153889857AG28GENIChomozygous112890497
4153897046153897047AC18GENIChomozygous112890499
4153897520153897521TC25GENIChomozygous112890500
4153898164153898165TC26GENIChomozygous112890501
4153898231153898232TC16GENIChomozygous112890502
4153899031153899032AC25GENIChomozygous112890503
4153901378153901379AG19GENIChomozygous112890504
4153902513153902514TA18GENIChomozygous112890505
4153902668153902669TC25GENIChomozygous112890507
4153903506153903507CT9GENIChomozygous112890508
4153904184153904185TC18GENIChomozygous112890509
4153904809153904810CT23GENIChomozygous112890511
4153905113153905114GT23GENIChomozygous112890512
4153905518153905519AG29GENIChomozygous112890513
4153905604153905605GA30GENIChomozygous112890514
4153905621153905622AG27GENIChomozygous112890516
4153905763153905764AG22GENIChomozygous112890517
4153906276153906277GA28GENIChomozygous112890519
4153907547153907548GC25GENIChomozygous112890520
4153907655153907656GA22GENICpossibly homozygous112890522
4153907937153907938TC11GENIChomozygous112890523
4153909904153909905GT17GENIChomozygous112890524
4153910480153910481CT14GENIChomozygous112890526
4153910676153910677GA28GENIChomozygous112890527
4153911639153911640GA15GENIChomozygous112890529
4153912012153912013TC23GENIChomozygous112890531