chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
62663660626636607TA9GENIChomozygous114747581
62663699126636992TG22GENICpossibly homozygous114747585
62663731526637316AC6GENIChomozygous114747587
62663732426637325TC5GENIChomozygous114747589
62663732526637326GA5GENIChomozygous114747591
62663734026637341AT18GENIChomozygous114747593
62663763726637638CT17GENICheterozygous115201712
62663805026638051TA20GENIChomozygous114747595
62663907726639078GT41GENIChomozygous114747599
62663912126639122CA39GENIChomozygous114747601
62664133526641336TA41GENIChomozygous114747605
62664133726641338AC42GENIChomozygous114747607
62664262726642628CG2GENIChomozygous114747609
62664351926643520CT29GENIChomozygous115493346
62664355826643559TC28GENIChomozygous115448130
62664444626644447TC32GENIChomozygous115448132
62664500826645009GA19GENIChomozygous115448134
62664597526645976GA39GENIChomozygous115493348
62664720826647209AC25GENIChomozygous115493350
62664722126647222GC25GENIChomozygous115493351
62664728426647285GA20GENIChomozygous115448138
62664728626647287AT20GENIChomozygous115448139
62664729926647300GA24GENIChomozygous115493353
62664856126648562CA48GENIChomozygous115448146
62664907226649073AG32GENIChomozygous115448148
62664917426649175CT30GENIChomozygous115493355