chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7121011833121011834GA23GENIChomozygous116409712
7121011992121011993CT15GENIChomozygous115857851
7121015693121015694GC28GENIChomozygous115857857
7121016117121016118CT26GENIChomozygous116409713
7121017119121017120CT40GENIChomozygous116409714
7121017705121017706TC25GENIChomozygous115857861
7121021885121021886GA54GENIChomozygous116409715
7121022031121022032GC29GENIChomozygous116409716
7121022418121022419CT51GENIChomozygous116409717
7121024509121024510TC4GENIChomozygous115857873
7121024732121024733AG29GENIChomozygous115857875
7121025096121025097AT3GENIChomozygous118393207
7121025786121025787GA31GENIChomozygous115857881
7121026339121026340TC7GENIChomozygous115857883
7121026448121026449TC9GENIChomozygous115857885
7121026478121026479TA8GENIChomozygous115857887
7121026563121026564TC15GENIChomozygous115857889
7121026566121026567AC15GENIChomozygous116081975
7121026567121026568GA15GENIChomozygous116081976
7121026614121026615AT28GENIChomozygous115857891
7121026779121026780AG28GENIChomozygous115857895
7121026868121026869TC33GENIChomozygous115857897
7121026912121026913GA34GENIChomozygous115857899
7121026981121026982CG37GENIChomozygous115857901
7121027114121027115GA22GENIChomozygous115857903
7121027147121027148TC22GENIChomozygous115857905
7121027156121027157AC26GENIChomozygous115857907
7121027182121027183AG32GENIChomozygous115857909
7121027229121027230TA38GENIChomozygous115857911
7121027273121027274GA31GENIChomozygous115857913
7121027361121027362TC35GENIChomozygous115857915
7121027830121027831GA25GENIChomozygous115857919
7121028300121028301AT23GENIChomozygous115857921