chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10104200678104200679CT12GENICheterozygous116961396
10104202321104202322TA7GENIChomozygous116834970
10104203121104203122CT6GENIChomozygous116961398
10104205439104205440TC9GENIChomozygous116834978
10104210915104210916TC18GENICheterozygous126391513
10104211377104211378GA27GENIChomozygous116834988
10104216653104216654CT11GENIChomozygous116961400
10104217046104217047AG14GENIChomozygous116834992
10104217065104217066TC11GENIChomozygous116834994
10104218485104218486TC18GENIChomozygous116961410
10104226293104226294CA3GENICheterozygous126425866
10104226579104226580GA10GENIChomozygous116961414
10104227502104227503GC10GENIChomozygous116961416
10104228128104228129CT5GENICheterozygous126425867
10104230756104230757AG10GENIChomozygous118070647
10104231546104231547CT17GENIChomozygous116961418
10104234963104234964CA28GENIChomozygous116961420
10104236521104236522AT11GENIChomozygous116983678
10104237387104237388GA6GENIChomozygous126391514
10104237639104237640TA13GENIChomozygous126391516
10104242142104242143AC13GENIChomozygous116961424
10104242738104242739AG15GENIChomozygous116835034
10104243177104243178AC17GENICheterozygous116961426
10104248827104248828TA22GENIChomozygous116835044
10104243400104243401CA18GENIChomozygous116961428
10104248703104248704GA8GENIChomozygous116835040
10104248785104248786AG19GENIChomozygous116835042
10104257587104257588AG4GENIChomozygous118070651
10104257588104257589CT4GENIChomozygous118070652