chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2207769303207769304TC46GENIChomozygous111363066
2207769400207769401TC35GENIChomozygous111363068
2207769746207769747GA39GENIChomozygous111363070
2207769779207769780TC32GENIChomozygous111363072
2207770443207770444AG30GENIChomozygous111363074
2207771223207771224TA29GENIChomozygous110217312
2207771334207771335CT25GENIChomozygous111363076
2207771495207771496CG29GENIChomozygous110217313
2207773195207773196GA32GENIChomozygous111363078
2207773440207773441GA18GENIChomozygous111363080
2207773468207773469GA19GENIChomozygous111363082
2207773730207773731TC35GENIChomozygous111363084
2207774607207774608AT25GENIChomozygous110217314
2207774685207774686TC22GENIChomozygous111363086
2207774787207774788CT21GENIChomozygous111363088
2207775116207775117TC28GENIChomozygous111363090
2207775203207775204CT23GENIChomozygous111363092
2207776140207776141GA48GENIChomozygous111363096
2207776195207776196TC35GENIChomozygous110217315
2207776693207776694AG31GENIChomozygous111363098
2207776765207776766TG29GENIChomozygous111363100
2207777050207777051TC27GENIChomozygous111363102
2207777142207777143CT30GENIChomozygous111363104
2207777265207777266TC32GENIChomozygous111363106
2207777360207777361AG22GENIChomozygous111363108
2207777844207777845GC24GENIChomozygous111363110
2207777939207777940CT28GENIChomozygous111363112
2207778186207778187TC24GENIChomozygous111363114
2207778260207778261TC24GENIChomozygous111363116
2207779557207779558CA38GENIChomozygous111363124
2207781683207781684TC26GENICpossibly homozygous111363126
2207782035207782036GT32GENIChomozygous111363128
2207782835207782836GC28GENIChomozygous111363130