chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X153555542153555543TG10GENIChomozygous962806448
X153598807153598808GA15GENIChomozygous962806449
X153598810153598811CA14GENIChomozygous962806450
X153598870153598871CA13GENIChomozygous962806451
X153602136153602137CT15GENIChomozygous962806452
X153602157153602158CT16GENIChomozygous962806453
X153602220153602221CT10GENIChomozygous962806454
X153692285153692286GC13GENICpossibly homozygous962806455
X153730959153730960GC21GENICheterozygous962806456
X153730961153730962AG21GENICheterozygous962806457
X153772165153772166GT18GENIChomozygous962806458
X153836513153836514TG10GENIChomozygous962806459