chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X5075808150758082TC9GENIChomozygous142755312
X5075819950758200GC10GENIChomozygous142755313
X5075828450758286GG7GENIChomozygous145972636
X5075860850758609GA8GENIChomozygous142755314
X5075868950758690GA9GENIChomozygous142755315
X5075878550758786AC7GENIChomozygous142755316
X5075880750758807TG9GENIChomozygous142743960
X5075901950759020CT11GENICpossibly homozygous142755317
X5075936950759370GT10GENIChomozygous142755318
X5075957150759572GA8GENIChomozygous142755319
X5075975150759751T7GENICpossibly homozygous142743961
X5075986250759863GA13GENIChomozygous142755320
X5075996050759961GC11GENIChomozygous142755321
X5076000550760006CT11GENIChomozygous142755322
X5076004250760043TA12GENIChomozygous142755323
X5076020150760202TC7GENIChomozygous142755324