chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5159590044159590045CT24GENIChomozygous958090582
5159590355159590356AC33GENIChomozygous958090583
5159590356159590357GC32GENIChomozygous958090584
5159590377159590378GA28GENIChomozygous958090585
5159590516159590517AG22GENIChomozygous958090586
5159590543159590544TC17GENIChomozygous958090587
5159590567159590568TC22GENIChomozygous958090588
5159590810159590811GA24GENIChomozygous958090589
5159591041159591042CT23GENIChomozygous958090590
5159591165159591166AG26GENIChomozygous958090591
5159591294159591295GA18GENIChomozygous958090592
5159591492159591493CT21GENIChomozygous958090593
5159591711159591712GA30GENIChomozygous958090594
5159591959159591960CT21GENIChomozygous958090595
5159592241159592242AG35GENIChomozygous958090596
5159592551159592552GA36GENIChomozygous958090597
5159592713159592714CT24GENIChomozygous958090598
5159593011159593012TA18GENIChomozygous958090599
5159593229159593230AG38GENIChomozygous958090600
5159593316159593317AC26GENIChomozygous958090601
5159594481159594482GA28GENIChomozygous958090602
5159595521159595522GA15GENIChomozygous958090603
5159598268159598269GA29GENIChomozygous958090604
5159599504159599505TC21GENIChomozygous958090605
5159600471159600472TC19GENIChomozygous958090606
5159601143159601144CT27GENIChomozygous958090607
5159601217159601218AG21GENIChomozygous958090608
5159601274159601275AG21GENIChomozygous958090609
5159602018159602019CT13GENIChomozygous958090610