chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
167446943874469439TC6GENIChomozygous111861089
167447107274471073TC11GENIChomozygous112032256
167448269274482693GA14GENIChomozygous112032258
167448295974482960CG11GENIChomozygous112032260
167448473074484731AG10GENIChomozygous111861091
167448649674486497CT12GENIChomozygous112032262
167449100374491004CT8GENICpossibly homozygous112032264
167449130874491309AG10GENIChomozygous111861095
167449742574497426CG13GENIChomozygous112032266
167449748174497482GC20GENIChomozygous112032268
167449804474498045TA8GENIChomozygous112032270
167449865674498657CT9GENIChomozygous111861099
167449866274498663TG10GENIChomozygous112032272
167449890374498904AG5GENIChomozygous112032274
167449893074498931AT5GENIChomozygous112032276
167449910874499109GA9GENIChomozygous112032279
167449958374499584CA4GENIChomozygous112032281