chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4153874951153874952TC16GENIChomozygous112890487
4153875716153875717AC29GENIChomozygous112890488
4153875760153875761GA32GENIChomozygous112890489
4153876544153876545GA34GENIChomozygous112890490
4153876607153876608GA25GENIChomozygous112890491
4153878243153878244TC10GENIChomozygous112890493
4153878862153878863AG20GENIChomozygous112890494
4153879296153879297GC13GENIChomozygous112890495
4153885866153885867TC32GENIChomozygous112890496
4153889856153889857AG26GENIChomozygous112890497
4153897046153897047AC33GENIChomozygous112890499
4153897520153897521TC20GENIChomozygous112890500
4153898164153898165TC32GENIChomozygous112890501
4153898231153898232TC26GENIChomozygous112890502
4153899031153899032AC31GENIChomozygous112890503
4153901378153901379AG21GENIChomozygous112890504
4153902513153902514TA24GENIChomozygous112890505
4153902668153902669TC27GENIChomozygous112890507
4153903506153903507CT20GENIChomozygous112890508
4153904184153904185TC23GENIChomozygous112890509
4153904650153904651GT37GENIChomozygous112890510
4153904809153904810CT31GENIChomozygous112890511
4153905113153905114GT19GENIChomozygous112890512
4153905518153905519AG22GENIChomozygous112890513
4153905604153905605GA23GENIChomozygous112890514
4153905621153905622AG27GENIChomozygous112890516
4153905763153905764AG26GENIChomozygous112890517
4153906276153906277GA28GENIChomozygous112890519
4153907547153907548GC24GENICpossibly homozygous112890520
4153907655153907656GA23GENIChomozygous112890522
4153909904153909905GT24GENIChomozygous112890524
4153910480153910481CT29GENIChomozygous112890526
4153910676153910677GA26GENIChomozygous112890527
4153911639153911640GA26GENIChomozygous112890529
4153912012153912013TC31GENIChomozygous112890531