chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104676917246769173TC23GENIChomozygous116586604
104676963346769634TC30GENIChomozygous116877940
104676984346769844GT34GENIChomozygous116877942
104677020346770204AG27GENIChomozygous116586608
104677288846772889TA28GENIChomozygous116877944
104677300146773002TC30GENIChomozygous116877946
104677309446773095GA33GENIChomozygous116586616
104677341546773416CT21GENIChomozygous116877948
104677776646777767CT21GENIChomozygous116877950
104677895146778952TA30GENIChomozygous116877952
104677986746779868AC30GENIChomozygous116877954
104678044646780447AG30GENIChomozygous116877956
104678131446781315CA23GENICpossibly homozygous116877958
104678280446782805AT8GENICheterozygous117103792
104678354046783541GA31GENIChomozygous116586638