chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5155465443155465444GA35GENIChomozygous515651273
5155466068155466071AAA---18GENIChomozygous689118124
5155466809155466810GT21GENIChomozygous515651274
5155466850155466851TG11GENIChomozygous515651275
5155466955155466956CG14GENIChomozygous517665136
5155467079155467080A-12GENIChomozygous689118126
5155467099155467100CT12GENIChomozygous515651276
5155467380155467381GT22GENIChomozygous515651277
5155467579155467580CA26GENIChomozygous515651278
5155467674155467675CA26GENIChomozygous515651279
5155467756155467757TC25GENICpossibly homozygous515651280
5155467773155467774GA26GENICpossibly homozygous515651281
5155467820155467821AG26GENIChomozygous515651282
5155468002155468003AG30GENIChomozygous515651283