chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
63542308735423088AAGAG7GENICheterozygous54349665
63542316735423168TC7GENIChomozygous54349667
63542343935423440TG17GENICpossibly homozygous54349670
63542431435424315CT27GENICpossibly homozygous54349673
63542476135424762GA22GENIChomozygous54349677
63542521135425213GG--11GENIChomozygous54349681
63542710335427104GGCTT6GENIChomozygous55957254
63542719135427192TC1GENIChomozygous54349683
63542719235427193GC2GENIChomozygous54349686
63542813435428135CA17GENIChomozygous54349689
63543210135432102CT16GENICpossibly homozygous54349697
63543218935432190AAT20GENIChomozygous54349699
63543239935432405AACAAC------4GENIChomozygous54349701
63543286835432869GA15GENICpossibly homozygous54349704
63543310835433109AG20GENICpossibly homozygous54349707
63543314735433148AG12GENIChomozygous54349710
63543442035434421GA21GENICpossibly homozygous54349713
63543618635436187CT17GENIChomozygous54349716
63543770435437705TC12GENIChomozygous54349719
63543832235438323GC25GENICpossibly homozygous54349722
63543949835439499AG16GENICpossibly homozygous54349725
63543986535439866GA19GENIChomozygous54349728
63543997835439979TTA3GENICheterozygous54349730