chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
123830377938303780GA17GENIChomozygous983166978
123830380938303810AC13GENIChomozygous983166979
123830422538304226GC10GENIChomozygous983166980
123830430038304301AG14GENIChomozygous983166981
123830433838304339GA17GENIChomozygous983166982
123830441238304413GA17GENIChomozygous983166983
123830456538304566GA21GENIChomozygous983166984
123830574238305743AC7GENIChomozygous983166985
123830773138307732CA34GENIChomozygous983166986
123830872838308729TC20GENIChomozygous983166987
123830878438308785AC18GENIChomozygous983166988
123830885538308856TC16GENIChomozygous983166989
123830904338309044CT12GENIChomozygous983166990
123830904438309045TA12GENIChomozygous983166991
123831550538315506AG14GENIChomozygous983166992
123831598838315989AG16GENIChomozygous983166993
123831851538318516TG15GENIChomozygous983166994
123831852838318529GT14GENIChomozygous983166995
123831919238319193CT23GENIChomozygous983166996
123831977738319778AG17GENIChomozygous983166997
123832412638324127CA24GENICpossibly homozygous983166998
123832542238325423AG16GENIChomozygous983166999
123832603738326038AG18GENIChomozygous983167000
123832666038326661TG17GENIChomozygous983167001
123832685438326855CG22GENIChomozygous983167002