chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104676917246769173TC26GENIChomozygous116586604
104676963346769634TC26GENICpossibly homozygous116877940
104676984346769844GT24GENIChomozygous116877942
104677020346770204AG30GENIChomozygous116586608
104677288846772889TA27GENIChomozygous116877944
104677300146773002TC22GENIChomozygous116877946
104677309446773095GA27GENIChomozygous116586616
104677341546773416CT30GENIChomozygous116877948
104677776646777767CT18GENIChomozygous116877950
104677895146778952TA21GENIChomozygous116877952
104677986746779868AC23GENIChomozygous116877954
104678044646780447AG39GENIChomozygous116877956
104678131446781315CA29GENICpossibly homozygous116877958
104678280446782805AT14GENICheterozygous117103792
104678354046783541GA18GENIChomozygous116586638