chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7143703523143703524TC50GENIChomozygous115944575
7143704191143704192CT36GENIChomozygous115944576
7143705011143705012CT65GENIChomozygous115944577
7143707516143707517AT33GENIChomozygous115944578
7143709101143709102GC44GENIChomozygous115944579
7143709129143709130TC45GENIChomozygous115944580
7143710452143710453AG41GENIChomozygous115944581
7143710934143710935GT56GENIChomozygous115944582
7143710937143710938GA58GENIChomozygous115944583
7143711222143711223CG43GENIChomozygous115944584
7143712309143712310GA36GENICpossibly homozygous115944585
7143712931143712932AG5GENIChomozygous115944586
7143716724143716725TC78GENIChomozygous115944587
7143718371143718372AG52GENIChomozygous115944588
7143718725143718726GC50GENIChomozygous115944589
7143719114143719115AG63GENIChomozygous115944590
7143719255143719256GC43GENIChomozygous115944591