chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
97188307871883079AG14GENIChomozygous941650627
97188492371884924GA17GENIChomozygous941650628
97188577971885780AG25GENIChomozygous941650629
97188693471886935AG32GENIChomozygous941650630
97188702471887025TG32GENIChomozygous941650631
97188755771887558TC30GENIChomozygous941650632
97188804471888045TG22GENIChomozygous941650633
97188974471889745CT13GENIChomozygous941650634
97189185871891859GA21GENIChomozygous941650635
97189261971892620GT16GENIChomozygous941650636
97189292171892922AG23GENIChomozygous941650637
97189358571893586AG22GENIChomozygous941650638
97189615071896151AC15GENIChomozygous941650639
97189864671898647AG18GENIChomozygous941650640
97190119571901196GA27GENIChomozygous941650641
97190135071901351TA22GENIChomozygous941650642
97190285471902855AG16GENIChomozygous941650643
97190289971902900GA21GENIChomozygous941650644
97190580771905808TC27GENIChomozygous941650645
97190597571905976GA27GENIChomozygous941650646
97190660071906601TC27GENIChomozygous941650647
97190719571907196GA27GENIChomozygous941650648
97190797271907973GA33GENIChomozygous941650649
97190823971908240TC20GENIChomozygous941650650
97190850071908501GA23GENIChomozygous941650651
97190853071908531TC24GENIChomozygous941650652
97190856971908570AG22GENIChomozygous941650653
97190867971908680AT18GENIChomozygous941650654
97190919271909193TC14GENIChomozygous941650655
97190963271909633CT21GENIChomozygous941650656
97191035071910351TC16GENIChomozygous941650657
97191035171910352TG16GENIChomozygous941650658
97191041171910412TC14GENIChomozygous941650659
97191066071910661GA29GENIChomozygous941650660
97191116171911162TA25GENIChomozygous941650661
97191131271911313GC21GENIChomozygous941650662