chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3149360460149360461GC11GENICheterozygous111772080
3149361659149361660GA6GENIChomozygous111772082
3149361889149361890CT7GENIChomozygous120112504
3149362438149362439GA15GENIChomozygous111772084
3149362814149362815TA14GENIChomozygous111772086
3149363479149363480CT24GENIChomozygous111772088
3149363908149363909AC16GENIChomozygous111772090
3149364628149364629GA24GENIChomozygous111772092
3149366075149366076GT15GENIChomozygous111772094
3149367075149367076TC12GENIChomozygous111772098
3149368566149368567CT8GENICheterozygous111772102
3149368732149368733AT25GENIChomozygous111772104
3149369431149369432CT8GENIChomozygous111772106
3149371580149371581GA21GENIChomozygous111772110
3149372475149372476GA14GENIChomozygous111772112
3149373026149373027CT4GENICheterozygous111772116
3149373273149373274GC10GENIChomozygous111772118
3149373454149373455GA20GENIChomozygous111772120
3149373779149373780GA15GENIChomozygous111772122
3149375312149375313AG12GENIChomozygous111772124
3149375321149375322TC9GENIChomozygous111772126
3149375457149375458CT17GENIChomozygous111772128
3149375587149375588AG16GENIChomozygous111772130
3149376454149376455TC14GENIChomozygous111772132
3149376677149376678AT9GENIChomozygous111772136
3149376876149376877CT13GENIChomozygous111772138
3149377007149377008AG11GENIChomozygous111772140
3149377061149377062TC14GENIChomozygous111772142
3149377076149377077CT12GENIChomozygous111772144
3149377197149377198GA4GENIChomozygous111772146
3149377732149377733GA12GENIChomozygous111772148
3149377838149377839CT15GENIChomozygous111772150