chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5159590044159590045CT22GENIChomozygous886363387
5159590377159590378GA5GENIChomozygous886363388
5159590516159590517AG10GENIChomozygous886363389
5159590543159590544TC17GENIChomozygous886363390
5159590567159590568TC13GENIChomozygous886363391
5159591041159591042CT14GENIChomozygous886363392
5159591165159591166AG12GENIChomozygous886363393
5159591294159591295GA10GENIChomozygous886363394
5159591492159591493CT15GENIChomozygous886363395
5159591711159591712GA21GENIChomozygous886363396
5159591959159591960CT12GENIChomozygous886363397
5159592241159592242AG14GENIChomozygous886363398
5159592551159592552GA18GENIChomozygous886363399
5159592593159592594GA22GENIChomozygous886363400
5159592713159592714CT13GENIChomozygous886363401
5159593011159593012TA9GENIChomozygous886363402
5159593229159593230AG11GENIChomozygous886363403
5159593316159593317AC8GENIChomozygous886363404
5159594481159594482GA15GENIChomozygous886363405
5159595521159595522GA16GENIChomozygous886363406
5159598268159598269GA20GENIChomozygous886363407
5159599504159599505TC25GENIChomozygous886363408
5159600471159600472TC14GENIChomozygous886363409
5159601143159601144CT18GENIChomozygous886363410
5159601217159601218AG12GENIChomozygous886363411
5159601274159601275AG13GENIChomozygous886363412
5159602018159602019CT8GENIChomozygous886363413