chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104678612446786125CT23GENIChomozygous116877960
104678673346786734CT23GENIChomozygous116877962
104678683446786835TC14GENIChomozygous116586642
104678784246787843CT25GENIChomozygous116586646
104678799146787992TC23GENIChomozygous116586648
104678965546789656GA17GENIChomozygous116586650
104678973746789738TC20GENIChomozygous116586652
104679126846791269CT19GENIChomozygous116586660
104679194146791942TA19GENIChomozygous116586664
104679200946792010TC20GENIChomozygous116586666
104679206046792061AG19GENIChomozygous116877964
104679259446792595GT25GENICpossibly homozygous116877966
104679301446793015CG22GENIChomozygous116586672
104679333146793332AG31GENIChomozygous116877968
104679392146793922CT22GENIChomozygous116877970
104679649046796491AT32GENIChomozygous116586678
104679726346797264CT33GENIChomozygous116877974
104679857546798576GA22GENIChomozygous116877976
104679935246799353TC26GENICpossibly homozygous116877978
104679957946799580GT19GENIChomozygous116877980
104679959346799594TC19GENIChomozygous116877982
104680138246801383GT24GENICpossibly homozygous116586684
104680139146801392AG26GENIChomozygous116586686
104680203246802033GC26GENIChomozygous116586688
104680316746803168GA39GENIChomozygous116877984
104680352846803529TC30GENIChomozygous116586692
104680407346804074GA13GENIChomozygous116586695
104680713246807133TC20GENIChomozygous116586701
104680839146808392TC22GENIChomozygous116586705
104680839546808396GA21GENIChomozygous116586707
104680869046808691CT25GENIChomozygous116877988
104680874446808745CA21GENIChomozygous116877991
104680895946808960AG24GENIChomozygous116586709
104680925146809252GA13GENIChomozygous116877993
104680928446809285TC15GENIChomozygous116586711
104680933546809336CA27GENIChomozygous116586713