chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71231731712317318TC48GENIChomozygous53790714
71231852912318530TG24GENICpossibly homozygous54711408
71231857612318580TTTG----17GENICheterozygous53790715
71231857712318580TTG---16GENICheterozygous53790716
71232090912320910TC20GENIChomozygous53790718
71232177212321773TG34GENIChomozygous54711410
71232203512322036GT31GENIChomozygous54711412
71232212912322130AAGT21GENIChomozygous54630143
71232264312322644CT29GENIChomozygous54711414
71232310212323104CT--30GENIChomozygous54711416
71232643612326437C-20GENIChomozygous54711418
71232708212327083GA56GENIChomozygous54711420
71233022612330227GA19GENIChomozygous54711422
71233135312331354GA38GENIChomozygous54711424
71233139912331400AG31GENIChomozygous53790727
71233152912331530CA24GENIChomozygous54711426
71233300912333010GA26GENIChomozygous54711428
71233332112333322GC28GENIChomozygous53790728
71233446512334466TTAC25GENICpossibly homozygous54630173
71233488012334881GA26GENIChomozygous54711430
71233514412335145GC31GENICheterozygous53790730
71233519512335196C-19GENICheterozygous53790731
71233521312335214AAC18GENICheterozygous53790732
71233558012335581AG28GENICheterozygous53790734
71233562312335624T-19GENICheterozygous53790735
71233564312335645CA--21GENICheterozygous53790736
71233698712336988GA23GENIChomozygous54711432
71233832112338322AATT22GENIChomozygous54181762
71233566712335668CT26GENICheterozygous54301818