chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1204562980204562981AG32GENICpossibly homozygous109364727
1204566513204566514TC28GENIChomozygous109364728
1204567283204567284TC25GENIChomozygous109364729
1204569016204569017AG21GENIChomozygous109364731
1204570650204570651CT37GENIChomozygous109364733
1204573696204573697GA27GENIChomozygous109364734
1204576162204576163TC5GENIChomozygous120875609
1204576815204576816TG46GENIChomozygous109364735
1204580764204580765AG36GENIChomozygous108515139