chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104749189247491893GA22GENIChomozygous52245336
104749249847492499TC37GENIChomozygous51445946
104749290647492907GA51GENIChomozygous51445947
104749291547492916TC45GENIChomozygous51445948
104749324247493243GA35GENIChomozygous51445949
104749339247493393TC38GENIChomozygous51445950
104749354347493544TC24GENIChomozygous51445951
104749354547493546AAG23GENIChomozygous51445952
104749372647493727GA26GENIChomozygous51445953
104749386547493866TC19GENIChomozygous51445954
104749390847493909TG31GENIChomozygous51445955
104749398147493982GA34GENIChomozygous51445956
104749401647494017GA37GENIChomozygous51445957
104749411347494114CT31GENIChomozygous51445958
104749440747494408CA25GENIChomozygous51445959
104749442147494422CG23GENIChomozygous51445960
104749457947494580GA19GENIChomozygous51445961
104749460147494616GGCTTTAATATCGGA---------------21GENIChomozygous51445962
104749485847494859G-11GENIChomozygous51445963
104749486547494868CCA---11GENICheterozygous52439141
104749486647494868CA--8GENICheterozygous51445965
104749498647494987CT32GENIChomozygous51445967
104749501847495019TC39GENIChomozygous51445968
104749533747495338CT25GENIChomozygous51445969
104749569447495695AG17GENIChomozygous51445970
104749647947496480AG27GENIChomozygous51445971
104749663547496636GA31GENIChomozygous51445972
104749685047496851GA37GENIChomozygous51445973
104749695447496955GA42GENIChomozygous51445974
104749713447497141GACTGAA-------12GENIChomozygous51445975
104749890347498904GA21GENICpossibly homozygous51445977
104749894147498942GA25GENICpossibly homozygous51445978
104749917847499179GA22GENIChomozygous51445979
104749918347499184CT23GENIChomozygous51445980