chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
86202135162021352TC9GENIChomozygous68747561
86202153762021538TG10GENIChomozygous68747565
86202211962022120TG15GENIChomozygous68747569
86202270662022707TC17GENIChomozygous68747573
86202380862023809AT16GENIChomozygous68747581
86202397762023978GA26GENIChomozygous68747585
86202447262024473GA11GENIChomozygous68747589
86202462862024629GA19GENIChomozygous68747594
86202519462025195TC4GENIChomozygous68747598
86202576762025768GT20GENIChomozygous68747618
86202678062026781CT17GENIChomozygous68747628
86202724062027241TC25GENIChomozygous68747632
86203090062030901CT9GENIChomozygous68747636
86203113262031133GA15GENIChomozygous68747639
86203244862032449AG5GENIChomozygous68747642
86203628762036288TC21GENIChomozygous68747650
86203782962037830GC20GENIChomozygous68747658
86203839562038396CT16GENIChomozygous68747662
86203963262039633TA6GENIChomozygous68747666
86204131162041312TC19GENIChomozygous68747674
86204224062042241TC4GENIChomozygous68747686
86204438862044389TC12GENIChomozygous68747690
86204478162044782AG13GENIChomozygous68747694
86204975662049757AG16GENIChomozygous68747698
86203655162036551C9GENIChomozygous69587183
86204035562040355A15GENICheterozygous69587185
86204443962044440A12GENIChomozygous69587187
86203881562038816A8GENIChomozygous69399760