chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104749249847492499TC18GENIChomozygous51445946
104749290647492907GA18GENIChomozygous51445947
104749291547492916TC16GENIChomozygous51445948
104749324247493243GA29GENIChomozygous51445949
104749339247493393TC24GENIChomozygous51445950
104749354347493544TC23GENIChomozygous51445951
104749354547493546AAG23GENIChomozygous51445952
104749372647493727GA22GENIChomozygous51445953
104749386547493866TC29GENIChomozygous51445954
104749390847493909TG19GENIChomozygous51445955
104749398147493982GA19GENIChomozygous51445956
104749401647494017GA27GENIChomozygous51445957
104749411347494114CT36GENIChomozygous51445958
104749440747494408CA31GENIChomozygous51445959
104749442147494422CG28GENIChomozygous51445960
104749457947494580GA24GENIChomozygous51445961
104749460147494616GGCTTTAATATCGGA---------------17GENIChomozygous51445962
104749485847494859G-2GENIChomozygous51445963
104749486647494868CA--2GENIChomozygous51445965
104749498647494987CT28GENIChomozygous51445967
104749501847495019TC25GENIChomozygous51445968
104749533747495338CT30GENIChomozygous51445969
104749569447495695AG27GENIChomozygous51445970
104749647947496480AG38GENIChomozygous51445971
104749663547496636GA29GENIChomozygous51445972
104749685047496851GA26GENIChomozygous51445973
104749695447496955GA23GENIChomozygous51445974
104749713447497141GACTGAA-------13GENIChomozygous51445975
104749890347498904GA14GENIChomozygous51445977
104749894147498942GA18GENIChomozygous51445978
104749917847499179GA26GENIChomozygous51445979
104749918347499184CT28GENIChomozygous51445980