chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5164038606164038607T-10GENIChomozygous55828092
5164040535164040536GA16GENICheterozygous55828093
5164040995164040996GA15GENICheterozygous56074846
5164042068164042069CT12GENICheterozygous55828094
5164045264164045265CG16GENIChomozygous55828099
5164045474164045475TC25GENIChomozygous55828100
5164045657164045658AG12GENICheterozygous56074854
5164046017164046018CG11GENIChomozygous55828101
5164046534164046535AC14GENICheterozygous55828102
5164047239164047240GA16GENICheterozygous56074856
5164047572164047573AT10GENICheterozygous55828103
5164047766164047767GC14GENICheterozygous55828104
5164048921164048922GA18GENICheterozygous55828105
5164049354164049355GA28GENIChomozygous55828106
5164049870164049871CA12GENIChomozygous55828107
5164050446164050447GGA17GENIChomozygous55828108
5164050641164050642AC13GENIChomozygous55828109
5164050682164050683TA15GENIChomozygous55828110
5164052047164052048CA13GENIChomozygous55828111
5164052521164052522GC17GENICheterozygous56074858
5164053610164053611AG25GENIChomozygous55828112
5164053931164053932AG23GENIChomozygous55828113
5164054099164054100CA25GENIChomozygous55828114
5164054234164054235CT14GENICheterozygous55828115
5164056683164056684AC15GENICheterozygous55828118
5164056947164056948CT19GENICheterozygous55828119
5164057199164057200AG15GENIChomozygous55828120
5164057329164057330AG24GENIChomozygous55828121
5164057375164057376CT26GENICheterozygous56074860
5164057841164057842TTA16GENICheterozygous56074862
5164058180164058181AG20GENIChomozygous55828122
5164058262164058263TC12GENIChomozygous55828123
5164061259164061260TC21GENICheterozygous56074864
5164061613164061614AG15GENIChomozygous55828124
5164061803164061804GA16GENICheterozygous55828125
5164064186164064187TC13GENIChomozygous55828128