chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
86202211962022120TG14GENIChomozygous68747569
86202270662022707TC14GENIChomozygous68747573
86202310862023109GA14GENIChomozygous69968392
86202356162023562AG12GENIChomozygous69968395
86202373062023731GA16GENIChomozygous69968398
86202593462025935TC12GENIChomozygous68747624
86203090062030901CT12GENIChomozygous68747636
86203469962034701AA13GENICheterozygous69968401
86203628762036288TC17GENIChomozygous68747650
86203782962037830GC19GENIChomozygous68747658
86203963262039633TA18GENIChomozygous68747666
86203997362039974GC22GENIChomozygous69968404
86204035562040355A24GENICheterozygous69968407
86204154362041544TA6GENIChomozygous68747678
86204154462041545AG7GENIChomozygous68747682
86204224062042241TC7GENIChomozygous68747686
86204232962042329T16GENICheterozygous69968410
86204438862044389TC19GENIChomozygous68747690
86204491362044914AT12GENIChomozygous69968413
86204519262045192A15GENICheterozygous69968416
86204529962045299AC6GENIChomozygous69968419
86204443962044440A10GENICheterozygous69587187
86203878962038790A6GENIChomozygous69664999
86203881562038816A4GENIChomozygous69399760
86204567062045671TC11GENIChomozygous68871491
86204652462046525CT18GENIChomozygous69968422
86204768462047685CG16GENIChomozygous68871495
86204844862048449GA19GENIChomozygous68871498
86204875462048755CG9GENIChomozygous69968425
86204875562048756TA9GENIChomozygous69968428
86204942162049422GA10GENIChomozygous68871500
86204975662049757AG17GENIChomozygous68747698
86205176462051765TC26GENIChomozygous68871504
86205191662051917GA20GENIChomozygous69968431