chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
109202549892025499CT25GENIChomozygous813212878
109202630292026303CT17GENIChomozygous813212879
109202677792026778CT16GENIChomozygous813212880
109202805992028060TA8GENIChomozygous813212881
109202810692028107AG14GENIChomozygous813212882
109202958992029590TA5GENICheterozygous813212883
109202976992029770AG8GENIChomozygous813212884
109202978292029783GA10GENIChomozygous813212885
109202989792029898AG20GENIChomozygous813212886
109202989992029900GT20GENIChomozygous813212887
109203073392030734TC26GENIChomozygous813212888
109203100092031001TA28GENIChomozygous813212889
109203102092031021CT30GENIChomozygous813212890
109203103692031037CA31GENICpossibly homozygous813212891
109203123192031232GA17GENIChomozygous813212892
109203135392031354AT23GENIChomozygous813212893
109203146792031468GC27GENIChomozygous813212894
109203165392031654TC20GENICpossibly homozygous813212895
109203272292032723CA27GENIChomozygous813212896
109203279492032795CT20GENIChomozygous813212897
109203300692033007TC23GENIChomozygous813212898
109203414092034141CG24GENIChomozygous813212899
109203443892034439CT29GENIChomozygous813212900
109203533192035332CG20GENIChomozygous813212901
109203732692037327CT32GENIChomozygous813212902
109203751992037520TC22GENIChomozygous813212903
109203954092039541GT21GENIChomozygous813212904
109204013492040135CT29GENIChomozygous813212905