chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
51451315914513160CT25GENIChomozygous113664937
51451395614513957GA19GENICpossibly homozygous113664939
51451495914514960TC22GENIChomozygous113664941
51451657514516576GA19GENIChomozygous113664945
51451676414516765TG10GENIChomozygous113664947
51451709314517094CA21GENIChomozygous113664949
51451710814517109TC21GENIChomozygous113664951
51451841214518413TC23GENIChomozygous113664953
51451865314518654GA23GENIChomozygous113664955
51451878814518789GA17GENIChomozygous113664957
51452032914520330CT21GENIChomozygous113664959
51452085114520852AG20GENICpossibly homozygous113664961
51452143114521432CG19GENIChomozygous113664963
51452153714521538GA24GENICpossibly homozygous113664965
51452154314521544GA23GENICpossibly homozygous113664967
51452195914521960CT15GENIChomozygous113664969
51452278614522787TC29GENIChomozygous113664971
51452394414523945AT34GENIChomozygous113664973
51452780514527806TC24GENIChomozygous113664981
51452855614528557TA30GENIChomozygous114108349
51452891814528919TC16GENIChomozygous113664983
51452987514529876TC22GENIChomozygous113664985
51453161214531613GT29GENIChomozygous113664991
51453256814532569GA14GENIChomozygous113664993
51453263914532640CT20GENIChomozygous113664995
51453368514533686CT25GENIChomozygous113664997
51453374314533744TC17GENIChomozygous113664999
51453464114534642GA27GENIChomozygous113665001
51453473614534737TA27GENIChomozygous113665003
51453614914536150GT11GENIChomozygous113665005
51453754614537547GA27GENIChomozygous113665007
51453760614537607TC28GENIChomozygous113665009
51453891514538916CT29GENICpossibly homozygous113665013
51453933514539336GA20GENIChomozygous113665015
51454136114541362TC19GENICpossibly homozygous113665017
51454179114541792AG23GENICpossibly homozygous113665021
51454444714544448AG13GENIChomozygous113665023
51454581114545812AG18GENICpossibly homozygous113665025
51454620514546206TC21GENIChomozygous113665027