chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
15103578245103578246TC21GENIChomozygous112630352
15103580229103580230CT18GENIChomozygous112630354
15103581543103581544GT15GENIChomozygous112630356
15103582491103582492TG11GENIChomozygous112630362
15103582583103582584AG19GENIChomozygous112630364
15103583347103583348CT19GENIChomozygous112630366
15103583379103583380TC15GENIChomozygous112630368
15103583590103583591AG17GENIChomozygous112630371
15103584931103584932TA11GENIChomozygous112630373
15103585919103585920GC21GENIChomozygous112630375
15103586107103586108CA20GENIChomozygous112630377
15103587372103587373AG21GENIChomozygous112630379
15103588386103588387AT15GENICheterozygous112630381
15103583039103583040TC9GENIChomozygous112827164