chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7129798708129798709CT15GENIChomozygous803544966
7129799658129799659GA27GENIChomozygous803544967
7129800613129800614CT27GENIChomozygous803544968
7129801117129801118AG27GENIChomozygous803544969
7129801936129801937GA21GENIChomozygous803544970
7129803953129803954CG24GENICpossibly homozygous803544971
7129804694129804695TG29GENIChomozygous803544972
7129804776129804777TC43GENIChomozygous803544973
7129804821129804822GA51GENIChomozygous803544974
7129805161129805162TC34GENICpossibly homozygous803544975
7129805282129805283AG34GENICpossibly homozygous803544976
7129805315129805316TC33GENIChomozygous803544977
7129805327129805328GT29GENIChomozygous803544978
7129805454129805455CA26GENICpossibly homozygous803544979
7129805486129805487TC36GENIChomozygous803544980
7129805522129805523TC41GENIChomozygous803544981
7129805543129805544GA34GENIChomozygous803544982
7129806000129806001CT15GENIChomozygous803544983
7129806589129806590CT27GENIChomozygous803544984
7129807333129807334GA23GENIChomozygous803544985
7129807636129807637CA27GENIChomozygous803544986
7129808777129808778CT20GENIChomozygous803544987
7129808911129808912GT20GENIChomozygous803544988
7129808987129808988AG27GENIChomozygous803544989
7129810320129810321TC20GENIChomozygous803544990
7129810349129810350TC24GENIChomozygous803544991
7129810795129810796CT18GENIChomozygous803544992
7129810829129810830GA15GENIChomozygous803544993
7129811223129811224AG28GENIChomozygous803544994