chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1236771653236771654GA25GENIChomozygous74764887
1236772084236772085TG20GENIChomozygous74764889
1236777755236777756CT6GENICheterozygous74764893
1236777759236777760CT6GENICheterozygous74764895
1236778717236778718GA28GENIChomozygous74764897
1236780173236780174GA10GENIChomozygous74764903
1236780647236780648TC23GENIChomozygous74764905
1236780650236780651TA23GENIChomozygous74764907
1236781120236781121GA30GENICpossibly homozygous74764909
1236785543236785544GA32GENIChomozygous74764911
1236785637236785638CT35GENIChomozygous74764913
1236791212236791213GC14GENIChomozygous74764915
1236796475236796476AG24GENIChomozygous74764917
1236798492236798493CT46GENIChomozygous74764919
1236799388236799389AG33GENIChomozygous74764921
1236801082236801083AC37GENIChomozygous74764923
1236808474236808475TC51GENIChomozygous74764925
1236809336236809337CT10GENICpossibly homozygous74764927
1236809340236809341CT9GENICpossibly homozygous74764929
1236809344236809345CT8GENICpossibly homozygous76669739
1236810265236810266CT9GENICheterozygous74764931
1236810551236810552CT14GENIChomozygous74764933
1236821621236821622AG21GENICheterozygous74764941
1236823053236823054CA29GENIChomozygous74764943
1236823800236823801CG37GENIChomozygous74764945
1236824752236824753TA34GENIChomozygous74764947
1236826500236826501TC31GENIChomozygous74764949
1236829146236829147GT51GENIChomozygous74764951
1236829942236829943CT48GENIChomozygous74764953
1236830994236830995AG16GENIChomozygous74764955
1236832667236832668CT28GENIChomozygous74764957
1236833597236833598AG14GENIChomozygous74764959
1236834023236834024CT20GENIChomozygous74764961
1236835029236835030TC35GENIChomozygous74764963
1236835361236835362TA6GENICheterozygous74764965
1236835799236835800CT37GENIChomozygous74764967
1236836206236836207GA63GENIChomozygous74764969
1236836356236836357AG42GENIChomozygous74764971
1236809348236809349CT5GENICheterozygous77822193