chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3175497099175497100CT20GENICpossibly homozygous112217965
3175501411175501412AG38GENIChomozygous112217966
3175502854175502855GT30GENIChomozygous112217967
3175503319175503320TG8GENIChomozygous112217968
3175504393175504394CA19GENIChomozygous112217969
3175506348175506349TC11GENICheterozygous119869493
3175507804175507805GT26GENIChomozygous112217970
3175508503175508504TC31GENIChomozygous112217971
3175508727175508728CT43GENIChomozygous112217972
3175508953175508954GA29GENIChomozygous112217973
3175510125175510126GA20GENIChomozygous112217974
3175510270175510271GT22GENIChomozygous112217975
3175510851175510852GA14GENIChomozygous112217976
3175511794175511795TC14GENIChomozygous112217977
3175512234175512235AC23GENIChomozygous112217978
3175513385175513386GA17GENIChomozygous112217979
3175513685175513686CA35GENIChomozygous112217980
3175514198175514199AG34GENIChomozygous112217981
3175516249175516250AC22GENIChomozygous112217982
3175516527175516528CT22GENIChomozygous112217983
3175516793175516794CG16GENIChomozygous112217984
3175517283175517284AG18GENIChomozygous112217985
3175518419175518420TG42GENIChomozygous112217986
3175521365175521366GA28GENIChomozygous112217989
3175525324175525325AT33GENIChomozygous119686712
3175526656175526657CT30GENIChomozygous112217990
3175526753175526754GC36GENIChomozygous112217991
3175527268175527269AG32GENIChomozygous112217992
3175529360175529361AG49GENIChomozygous112217993
3175530144175530145GA23GENIChomozygous112217994
3175534154175534155CT25GENIChomozygous112217995
3175534733175534734GT24GENIChomozygous112217996
3175534856175534857CA31GENIChomozygous112217997
3175535234175535235TC28GENIChomozygous112217998
3175538873175538874GA23GENIChomozygous112217999