chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1236771653236771654GA16GENIChomozygous74764887
1236772084236772085TG23GENIChomozygous74764889
1236777755236777756CT6GENICheterozygous74764893
1236777759236777760CT6GENICheterozygous74764895
1236778717236778718GA18GENICheterozygous74764897
1236780173236780174GA11GENIChomozygous74764903
1236780647236780648TC17GENIChomozygous74764905
1236780650236780651TA16GENIChomozygous74764907
1236781120236781121GA13GENICpossibly homozygous74764909
1236785543236785544GA18GENIChomozygous74764911
1236785637236785638CT20GENIChomozygous74764913
1236791212236791213GC18GENIChomozygous74764915
1236796475236796476AG21GENIChomozygous74764917
1236798492236798493CT30GENIChomozygous74764919
1236799388236799389AG19GENIChomozygous74764921
1236801082236801083AC15GENIChomozygous74764923
1236808474236808475TC23GENIChomozygous74764925
1236809336236809337CT3GENIChomozygous74764927
1236809340236809341CT3GENIChomozygous74764929
1236810265236810266CT4GENICheterozygous74764931
1236810551236810552CT19GENIChomozygous74764933
1236823053236823054CA18GENIChomozygous74764943
1236823800236823801CG26GENIChomozygous74764945
1236824752236824753TA19GENIChomozygous74764947
1236826500236826501TC17GENIChomozygous74764949
1236829146236829147GT34GENIChomozygous74764951
1236829942236829943CT29GENIChomozygous74764953
1236830994236830995AG22GENIChomozygous74764955
1236832667236832668CT25GENIChomozygous74764957
1236833597236833598AG11GENIChomozygous74764959
1236834023236834024CT13GENIChomozygous74764961
1236835029236835030TC17GENIChomozygous74764963
1236835799236835800CT27GENIChomozygous74764967
1236836206236836207GA32GENIChomozygous74764969
1236836356236836357AG25GENIChomozygous74764971