chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1101465951101465952GA11GENIChomozygous108900485
1101466120101466121GA18GENIChomozygous108900487
1101467183101467184GA33GENIChomozygous108900492
1101469032101469033CT16GENICpossibly homozygous108900494
1101469574101469575CG28GENIChomozygous108900496
1101469645101469646AG25GENIChomozygous108900498
1101474429101474430AG20GENIChomozygous108900503
1101474870101474871GA23GENIChomozygous108900505
1101474914101474915GA23GENIChomozygous108900507
1101475293101475294TC31GENIChomozygous108900509
1101475953101475954AC17GENIChomozygous108900511
1101476043101476044TC21GENIChomozygous108900512