chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7121011992121011993CT19GENIChomozygous115857851
7121015693121015694GC34GENIChomozygous115857857
7121017222121017223CT31GENIChomozygous116224888
7121017546121017547AT34GENIChomozygous116224889
7121023606121023607CG29GENIChomozygous116224890
7121023672121023673GT28GENIChomozygous115857869
7121024509121024510TC22GENIChomozygous115857873
7121024732121024733AG21GENIChomozygous115857875
7121024775121024776CT24GENIChomozygous116224891
7121025128121025129AT4GENIChomozygous115857879
7121025661121025662GA26GENIChomozygous116224892
7121026243121026244GA23GENIChomozygous116224893
7121026339121026340TC8GENIChomozygous115857883
7121026448121026449TC19GENIChomozygous115857885
7121026563121026564TC21GENIChomozygous115857889
7121026614121026615AT35GENIChomozygous115857891
7121026778121026779CT33GENIChomozygous115857893
7121026779121026780AG32GENIChomozygous115857895
7121026868121026869TC38GENIChomozygous115857897
7121026912121026913GA32GENIChomozygous115857899
7121026981121026982CG31GENIChomozygous115857901
7121027114121027115GA36GENIChomozygous115857903
7121027147121027148TC30GENIChomozygous115857905
7121027156121027157AC37GENIChomozygous115857907
7121027182121027183AG31GENIChomozygous115857909
7121027229121027230TA29GENIChomozygous115857911
7121027361121027362TC30GENIChomozygous115857915
7121027645121027646AG11GENIChomozygous115857917
7121027830121027831GA29GENIChomozygous115857919
7121028003121028004GA33GENIChomozygous116224894
7121028300121028301AT33GENIChomozygous115857921