chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
98806413188064132TG42GENICpossibly homozygous144409208
98806454088064541T39GENICpossibly homozygous144400811
98806506188065062TA57GENIChomozygous144409209
98806507088065071CA59GENIChomozygous144409210
98806521888065221AGA53GENICpossibly homozygous144400812
98806574588065746A39GENICpossibly homozygous138472799
98806657188066572AT58GENIChomozygous144409211
98806687788066878GA45GENIChomozygous144409212
98806911088069111GA47GENIChomozygous144409213
98806914588069146AG49GENIChomozygous144409214
98806976488069765T52GENIChomozygous144400813
98807011688070117CT68GENIChomozygous138622041
98807053088070531GA58GENIChomozygous144409215
98807063188070632GA57GENIChomozygous144409216
98807094588070946AG60GENIChomozygous144409217
98806921688069217GT48GENIChomozygous143418002