chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7130080883130080884TG24GENICpossibly homozygous54110272
7130081417130081418AC27GENIChomozygous54110273
7130081711130081719TTCATGTG--------2GENIChomozygous54110274
7130081826130081827AG6GENICheterozygous54110275
7130082062130082063TA19GENICpossibly homozygous54110276
7130082104130082105GA18GENIChomozygous54110277
7130083749130083751GT--3GENIChomozygous54110278
7130084679130084680AAT6GENICheterozygous54110279
7130084956130084957GA8GENIChomozygous54110281
7130087034130087035CT10GENIChomozygous54110283
7130087037130087038TC9GENIChomozygous54110284
7130087898130087899AT24GENIChomozygous54110285
7130088333130088334CT20GENICpossibly homozygous54110286