chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2249540394249540395TC13GENIChomozygous110374951
2249540807249540808TA21GENIChomozygous110374953
2249541077249541078CA21GENIChomozygous110374955
2249542938249542939CA23GENIChomozygous110374959
2249542971249542972AC30GENIChomozygous110374961
2249543149249543150CT22GENIChomozygous110374963
2249543193249543194CA25GENIChomozygous110374965
2249543292249543293CA34GENIChomozygous110374967
2249543489249543490AG28GENIChomozygous110374969
2249543601249543602TC33GENIChomozygous110374971
2249543760249543761GA26GENIChomozygous110374973
2249544521249544522GA37GENIChomozygous110374975
2249544768249544769CT27GENIChomozygous110374977
2249544805249544806GA26GENIChomozygous110374979
2249544918249544919CT17GENIChomozygous110374980
2249545081249545082GA23GENIChomozygous110374982
2249545213249545214TC27GENIChomozygous110374984
2249545462249545463CT31GENIChomozygous110374986
2249546937249546938CT32GENIChomozygous110374988
2249547385249547386TC28GENIChomozygous110374990
2249547706249547707GA30GENIChomozygous110374992
2249549440249549441CT27GENIChomozygous110374994
2249549634249549635AG21GENIChomozygous110374996
2249550507249550508AG18GENIChomozygous110374998
2249550685249550686TC24GENIChomozygous110375000
2249551133249551134AG27GENIChomozygous110375002
2249551482249551483GA32GENICpossibly homozygous110375004