chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
99423873494238735TC53GENIChomozygous781322990
99423878194238782TC42GENIChomozygous781322991
99423891794238918GA55GENIChomozygous781322992
99423896394238964AG49GENIChomozygous781322993
99423900194239002CT54GENIChomozygous781322994
99423913494239135GA46GENIChomozygous781322995
99423918894239189TC37GENIChomozygous781322996
99423932694239327GA47GENIChomozygous781322997
99424098994240990CT101GENICpossibly homozygous781322998
99424207294242073GC61GENICpossibly homozygous781322999
99424233294242333AG72GENICpossibly homozygous781323000
99424236494242365AC66GENIChomozygous781323001
99424429794244298GC58GENIChomozygous781323002
99424750794247508GA55GENIChomozygous781323003
99424763094247631AC47GENIChomozygous781323004
99424796994247970AG45GENIChomozygous781323005
99424805794248058AT62GENIChomozygous781323006
99424848494248485CG44GENICpossibly homozygous781323007
99424942394249424TC74GENIChomozygous781323008
99425083194250832CT54GENIChomozygous781323009
99425212494252125AG69INTERGENIChomozygous781323010