chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
114546274645462747TG16GENIChomozygous115854087
114546289345462894GA13GENIChomozygous115854089
114546290745462908CT15GENIChomozygous115854091
114546293845462939CT14GENIChomozygous115854093
114546302545463026TA16GENIChomozygous115854095
114546322045463221TC24GENIChomozygous115854097
114546346645463467AT23GENIChomozygous115963446
114546346745463468GA24GENIChomozygous115854099
114546377045463771TG32GENIChomozygous115854101
114546378745463788TC36GENIChomozygous115854103
114546412245464123GA28GENIChomozygous115854105
114546417345464174CT38GENIChomozygous115854107
114546491345464914CT42GENIChomozygous115854109
114546510045465101GA33GENIChomozygous115854111
114546570745465708CT36GENIChomozygous115854113
114546596445465965GA20GENIChomozygous115854115
114546712645467127AC35GENIChomozygous115854117
114546755345467554TC26GENIChomozygous115854119
114546797345467974GA21GENIChomozygous115854121
114546823745468238CG30GENIChomozygous115854123
114546825945468260AG29GENIChomozygous115854125
114546835645468357TC25GENIChomozygous115854127
114546911845469119TC21GENIChomozygous115854129
114546934045469341TG24GENIChomozygous115854131
114546951445469515TG20GENIChomozygous115854133
114546998845469989TC21GENIChomozygous115854135
114547013345470134GA29GENIChomozygous115854137
114547038245470383CT30GENIChomozygous115854139
114547044345470444GA31GENIChomozygous115854141
114547107745471078TC29GENIChomozygous115854143
114547185445471855AT28GENIChomozygous115854147
114547186945471870GA25GENIChomozygous115854149
114547236045472361CT32GENICpossibly homozygous115854151