chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
118404190184041902GA29GENIChomozygous116069066
118404214684042147AG21GENIChomozygous116069068
118404219884042199AG22GENIChomozygous116069071
118404250784042508TC13GENIChomozygous118210161
118404252484042524CGCT12GENIChomozygous132157790
118404252984042531AT14GENIChomozygous132157791
118404311984043120CT16GENIChomozygous116069073
118404312784043128CT15GENIChomozygous116069075
118404392484043927CCG8GENICheterozygous132335158
118404393084043931CA9GENIChomozygous116250148
118404394184043942AG10GENIChomozygous116207739
118404407284044073GA14GENIChomozygous116069077
118404417084044171GC16GENIChomozygous116069079
118404417184044172GC15GENIChomozygous116069081
118404420284044203CG17GENIChomozygous116069083
118404493484044935TA32GENIChomozygous116069085
118404511284045113GC16GENIChomozygous116069087
118404603784046038AG28GENIChomozygous116069089
118404618384046184TG18GENIChomozygous116069091
118404648784046488CT24GENIChomozygous116069093
118404667984046680A23GENIChomozygous128930462
118404668884046689AT24GENIChomozygous116207741
118404669284046693AT24GENIChomozygous116207743
118404669784046698A23GENIChomozygous132157792
118404670584046706AT21GENIChomozygous116267239
118404671384046723AAAAATATAT20GENIChomozygous132157793
118404739184047392CT22GENIChomozygous116069095
118404740884047409CG23GENIChomozygous116207745