chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3149360460149360461GC17GENIChomozygous111772080
3149361659149361660GA12GENIChomozygous111772082
3149362438149362439GA11GENIChomozygous111772084
3149362814149362815TA6GENIChomozygous111772086
3149363479149363480CT10GENIChomozygous111772088
3149363908149363909AC13GENIChomozygous111772090
3149364628149364629GA10GENIChomozygous111772092
3149366075149366076GT7GENIChomozygous111772094
3149366106149366107CT6GENIChomozygous111772096
3149367075149367076TC14GENIChomozygous111772098
3149368566149368567CT20GENICpossibly homozygous111772102
3149368732149368733AT12GENIChomozygous111772104
3149369431149369432CT12GENIChomozygous111772106
3149371580149371581GA14GENICpossibly homozygous111772110
3149372475149372476GA9GENIChomozygous111772112
3149373014149373015GT5GENIChomozygous111772114
3149373026149373027CT4GENIChomozygous111772116
3149373273149373274GC6GENIChomozygous111772118
3149373779149373780GA8GENIChomozygous111772122
3149375312149375313AG9GENIChomozygous111772124
3149375321149375322TC9GENIChomozygous111772126
3149375457149375458CT6GENIChomozygous111772128
3149375587149375588AG10GENIChomozygous111772130
3149376677149376678AT8GENIChomozygous111772136
3149376876149376877CT14GENIChomozygous111772138
3149377007149377008AG12GENIChomozygous111772140
3149377061149377062TC14GENIChomozygous111772142
3149377076149377077CT14GENIChomozygous111772144
3149377732149377733GA7GENIChomozygous111772148
3149377838149377839CT10GENIChomozygous111772150