chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7121351511121351512AC7GENIChomozygous877268839
7121351659121351660AG15GENIChomozygous877268840
7121351666121351667GA17GENIChomozygous877268841
7121352112121352113AG25GENIChomozygous877268842
7121352821121352822AG7GENIChomozygous877268843
7121354407121354408AG9GENIChomozygous877268844
7121354414121354415CT8GENIChomozygous877268845
7121354892121354893AC12GENIChomozygous877268846
7121357005121357006TG31GENIChomozygous877268847
7121364820121364821CT16GENIChomozygous877268853
7121365351121365352AG6GENIChomozygous877268854
7121365669121365670TC16GENIChomozygous877268855
7121367352121367353TC7GENIChomozygous877268856
7121367375121367376GA10GENIChomozygous877268857
7121369373121369374AG18GENIChomozygous877268858
7121370431121370432TC22GENIChomozygous877268859
7121370678121370679CT25GENIChomozygous877268860
7121371103121371104GA10GENIChomozygous877268861
7121372869121372870TC27GENIChomozygous877268862
7121373043121373044TC11GENIChomozygous877268863
7121374131121374132AG20GENIChomozygous877268864
7121374767121374768CT14GENIChomozygous877268865
7121376233121376234TC16GENIChomozygous877268866
7121376634121376635TC8GENICheterozygous877268867
7121377740121377741CT21GENIChomozygous877268868
7121378332121378333TC27GENIChomozygous877268869
7121379448121379449GA18GENIChomozygous877268870
7121380634121380635TC22GENIChomozygous877268871
7121381943121381944TC9GENIChomozygous877268872
7121382028121382029GA33GENIChomozygous877268873