chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4153922655153922656CG28GENIChomozygous112890551
4153923647153923648TC30GENIChomozygous112890552
4153924642153924643GA24GENIChomozygous112890554
4153924966153924967AC12GENICpossibly homozygous112890555
4153930636153930637AG28GENIChomozygous112890558
4153931649153931650GA29GENIChomozygous112890564
4153931955153931956TA24GENIChomozygous112890566
4153933335153933336CT24GENIChomozygous112890567
4153933430153933431AC20GENIChomozygous112890569
4153934973153934974GC6GENICheterozygous119456133
4153934976153934977TC9GENICheterozygous119456134
4153937737153937738AG31GENICpossibly homozygous112890570
4153938818153938819TG28GENIChomozygous112890572
4153939806153939807CA20GENICpossibly homozygous112890573
4153941047153941048CT13GENIChomozygous112890575