chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
181788215217882153GT29GENIChomozygous110289765
181788636317886364AG11GENIChomozygous110453773
181789195617891957CT26GENIChomozygous110289769
181789301517893016CT34GENIChomozygous110289771
181789349817893499CG19GENIChomozygous110289773
181789367117893672TC26GENIChomozygous110289775
181789375517893756GC28GENICpossibly homozygous110289777
181789628017896281CT23GENIChomozygous110289779
181789682017896821TC31GENICpossibly homozygous110577312
181789713217897133GA20GENICpossibly homozygous110289781
181789842917898430CA26GENIChomozygous110289783
181789844317898444GT26GENIChomozygous110289785
181789844717898448CT26GENIChomozygous110289787
181789845117898452CT25GENIChomozygous110289789
181789845517898456CT24GENIChomozygous110289791
181789845717898458CT24GENIChomozygous110289793
181789846517898466CT22GENIChomozygous110289795
181790063217900633CT17GENIChomozygous110289797
181790090217900903TC33GENIChomozygous110289799
181790174717901748TG28GENICpossibly homozygous110289801
181790295617902957AG18GENICpossibly homozygous110289803
181790345417903455GA14GENIChomozygous110289805
181790359917903600AT25GENIChomozygous110289807
181790364517903646TC25GENIChomozygous110289809
181790365317903654TC24GENIChomozygous110289811
181790373017903731GA20GENIChomozygous110289813
181790388117903882AG33GENIChomozygous110577314
181790390317903904GT26GENIChomozygous110577316
181790574017905741GA22GENICpossibly homozygous110289819
181790779117907792GA27GENIChomozygous110289821
181790789217907893TC33GENIChomozygous110289823
181790913317909134TC32GENIChomozygous110289825
181790917017909171GA29GENIChomozygous110289827
181790960717909608AG24GENICpossibly homozygous110289829
181791048517910486AT23GENICpossibly homozygous110289831
181791234217912343CA27GENICpossibly homozygous110289833
181791284417912845GA29GENIChomozygous110289835
181790153817901539CT12GENIChomozygous110915625