chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
64648571146485712TG22GENIChomozygous637811540
64648590746485908AT22GENIChomozygous637811541
64648611546486116TTC11GENIChomozygous749598701
64648654346486544GC17GENIChomozygous637811542
64648729846487299CT39GENIChomozygous637811543
64648740146487402CT28GENIChomozygous637811544
64648770946487710CCT14GENICpossibly homozygous749598703
64648778746487788AG22GENIChomozygous637811545
64648785446487855G-18GENIChomozygous749598704
64648813746488138AACGCG28GENIChomozygous749598705
64648814246488143CT23GENIChomozygous637811546
64648858946488590AG23GENIChomozygous637811547
64648864946488650CG21GENIChomozygous637811548
64648870146488702TC20GENIChomozygous637811549
64648894846488949GA27GENIChomozygous637811550
64648910046489101GC31GENIChomozygous637811551
64648971946489720CT47GENIChomozygous637811552
64648975046489751CG42GENIChomozygous637811553
64648980046489801AG44GENIChomozygous637811554
64648981546489816CT35GENIChomozygous637811555
64648990546489906G-31GENIChomozygous749598706
64648992646489927CT32GENIChomozygous637811556