chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
75421344154213442CT16GENIChomozygous115686618
75421423654214237CT49GENICpossibly homozygous115686619
75421593354215934TC30GENIChomozygous115686620
75421862654218627GA52GENIChomozygous115686621
75421977354219774TA40GENIChomozygous115686622
75422034254220343CT15GENIChomozygous115686623
75422195254221953GA38GENIChomozygous115686624
75422247954222480TC51GENIChomozygous115686625
75422373254223733CA23GENIChomozygous115686626
75422410454224105GA38GENIChomozygous115686627
75422473154224732AG31GENIChomozygous115686628
75423053254230533CT54GENIChomozygous115686629
75423055154230552TC46GENIChomozygous115686630
75423208454232085CT22GENIChomozygous115686631
75423211654232117TG26GENIChomozygous115686632
75423343054233431TG38GENICheterozygous115686633
75423417654234177AG26GENIChomozygous115686634
75423451854234519GA28GENIChomozygous115686635
75423515454235155CT26GENIChomozygous115686636
75423523654235237TG22GENIChomozygous115686637
75423638854236389AG25GENIChomozygous115686638