chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
115884830358848304GA29GENIChomozygous115875862
115888069558880696TC20GENIChomozygous115875864
115896360058963601GT17GENIChomozygous115875866
115896395558963956CA30GENIChomozygous115875868
115896396558963966TA33GENIChomozygous115875870
115897279458972795TA19GENIChomozygous115875872
115897998658979987TG47GENIChomozygous115875874
115897999258979993CT44GENIChomozygous115875876
115897999458979995TA43GENIChomozygous115875878
115904551959045520TC9GENICheterozygous115875880
115904552359045524AT9GENICheterozygous115875882
115908679259086793GC28GENIChomozygous115875884
115909271559092716CG22GENIChomozygous115875886
115912214759122148AG24GENIChomozygous115875888
115914986659149867GA34GENIChomozygous115875890
115919159359191594AT17GENIChomozygous115875892
115919159459191595AG17GENIChomozygous115875894
115919159559191596GC17GENIChomozygous115875896
115927864959278650GT24GENIChomozygous115875898
115928617259286173CT25GENIChomozygous115875900
115937084859370849CA10GENIChomozygous115875902
115937084959370850CA10GENIChomozygous115875904
115937217559372176GT17GENICheterozygous115875906
115937217759372178AT13GENICheterozygous115875908
115937868959378690AC15GENIChomozygous115875910
115937869059378691CA16GENIChomozygous115875912
115937885859378859CA18GENIChomozygous115875914
115940165259401653AG21GENIChomozygous115875916