chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104678612446786125CT30GENIChomozygous116877960
104678673346786734CT17GENIChomozygous116877962
104678683446786835TC24GENIChomozygous116586642
104678784246787843CT32GENIChomozygous116586646
104678799146787992TC15GENIChomozygous116586648
104678965546789656GA14GENIChomozygous116586650
104678973746789738TC31GENIChomozygous116586652
104679126846791269CT21GENIChomozygous116586660
104679194146791942TA22GENIChomozygous116586664
104679200946792010TC32GENIChomozygous116586666
104679206046792061AG18GENIChomozygous116877964
104679259446792595GT22GENIChomozygous116877966
104679301446793015CG16GENIChomozygous116586672
104679333146793332AG36GENIChomozygous116877968
104679392146793922CT21GENIChomozygous116877970
104679478546794786CT12GENIChomozygous116877972
104679649046796491AT41GENIChomozygous116586678
104679726346797264CT24GENIChomozygous116877974
104679857546798576GA34GENIChomozygous116877976
104679935246799353TC24GENIChomozygous116877978
104679957946799580GT23GENIChomozygous116877980
104679959346799594TC26GENIChomozygous116877982
104680138246801383GT34GENICpossibly homozygous116586684
104680139146801392AG33GENIChomozygous116586686
104680203246802033GC31GENIChomozygous116586688
104680316746803168GA36GENIChomozygous116877984
104680352846803529TC23GENIChomozygous116586692
104680407346804074GA29GENIChomozygous116586695
104680490746804908AG11GENIChomozygous116877986
104680713246807133TC31GENIChomozygous116586701
104680839146808392TC23GENIChomozygous116586705
104680839546808396GA22GENIChomozygous116586707
104680869046808691CT21GENIChomozygous116877988
104680874446808745CA23GENIChomozygous116877991
104680895946808960AG36GENIChomozygous116586709
104680925146809252GA31GENIChomozygous116877993
104680928446809285TC32GENIChomozygous116586711
104680933546809336CA23GENIChomozygous116586713