chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5159590044159590045CT28GENIChomozygous966883410
5159590355159590356AC24GENIChomozygous966883411
5159590356159590357GC24GENIChomozygous966883412
5159590377159590378GA24GENIChomozygous966883413
5159590516159590517AG16GENIChomozygous966883414
5159590543159590544TC19GENIChomozygous966883415
5159590567159590568TC16GENIChomozygous966883416
5159590810159590811GA21GENIChomozygous966883417
5159591041159591042CT18GENIChomozygous966883418
5159591165159591166AG36GENIChomozygous966883419
5159591294159591295GA37GENIChomozygous966883420
5159591492159591493CT19GENIChomozygous966883421
5159591711159591712GA23GENIChomozygous966883422
5159591959159591960CT29GENIChomozygous966883423
5159592241159592242AG33GENIChomozygous966883424
5159592551159592552GA36GENIChomozygous966883425
5159592593159592594GA42GENIChomozygous966883426
5159592713159592714CT32GENIChomozygous966883427
5159593011159593012TA21GENIChomozygous966883428
5159593229159593230AG38GENIChomozygous966883429
5159593316159593317AC41GENIChomozygous966883430
5159594481159594482GA34GENIChomozygous966883431
5159595521159595522GA26GENIChomozygous966883432
5159598268159598269GA26GENIChomozygous966883433
5159599504159599505TC23GENIChomozygous966883434
5159600471159600472TC18GENIChomozygous966883435
5159601143159601144CT23GENIChomozygous966883436
5159601217159601218AG33GENIChomozygous966883437
5159601274159601275AG32GENIChomozygous966883438
5159602018159602019CT16GENIChomozygous966883439