chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X109940936109940937CT5GENIChomozygous108715266
X109942430109942431CT14GENIChomozygous108598027
X109942828109942829AT10GENIChomozygous108715268
X109943648109943649GA13GENIChomozygous108715270
X109945065109945066GT13GENIChomozygous108598029
X109945421109945422AC10GENIChomozygous108598031
X109946443109946444AG14GENIChomozygous108715272
X109946495109946496GT22GENIChomozygous108598033
X109949205109949206CT15GENIChomozygous108715274
X109955086109955087GA15GENIChomozygous108715276
X109955265109955266GT9GENIChomozygous108715278
X109956522109956523GC11GENIChomozygous108715280
X109959319109959320AG13GENIChomozygous108308643