chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
65077330350773304AT4GENIChomozygous972733116
65077445950774460AG17GENIChomozygous972733117
65077452650774527TC16GENIChomozygous972733118
65077597650775977GA20GENIChomozygous972733119
65077644450776445CT18GENIChomozygous972733120
65077671050776711CT16GENIChomozygous972733121
65077698850776989GA19GENIChomozygous972733122
65077786450777865GA4GENIChomozygous972733123
65077907450779075CT16GENIChomozygous972733124
65077909450779095AG15GENIChomozygous972733125
65078189350781894AG12GENIChomozygous972733126
65078208950782090TC20GENIChomozygous972733127
65078330950783310AG28GENIChomozygous972733128
65078338050783381AT27GENIChomozygous972733129
65078358850783589AG19GENICpossibly homozygous972733130