chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
107291199172911992GA15GENIChomozygous116633282
107291232472912325CT17GENIChomozygous117085028
107291273072912731AT8GENIChomozygous116800098
107291278172912782CG9GENIChomozygous116633284
107291278672912787AC9GENIChomozygous116633286
107291310572913106TC6GENIChomozygous116633288
107291340272913403TC9GENIChomozygous116633290
107291990572919906CT9GENIChomozygous117085036
107291643272916433GA28GENIChomozygous117085032
107291788872917889GA20GENIChomozygous117085034
107292052872920529AT18GENIChomozygous116633294
107292060872920609AC17GENIChomozygous116633296
107292611672926117AC30GENIChomozygous116633300
107292670772926708CT20GENIChomozygous117104623
107292865572928656CT13GENIChomozygous117085044
107293010272930103CT15GENIChomozygous117085046
107293124872931249TG17GENIChomozygous116633304
107293142172931422CT34GENIChomozygous116633306
107293178072931781AT15GENIChomozygous116633308
107293192272931923AG16GENIChomozygous116633310
107293294872932949AG17GENIChomozygous116633312
107293338672933387TC17GENIChomozygous116633314
107293781572937816CT13GENIChomozygous116633324
107294005472940055TC3GENIChomozygous117344888
107294169672941697TG9GENIChomozygous116633326
107294364072943641GA29GENIChomozygous116633334
107294411872944119GT15GENIChomozygous116633336
107294442472944425TC18GENIChomozygous116633338