chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
107291185872911859CA11GENIChomozygous117085026
107291199172911992GA25GENIChomozygous116633282
107291232472912325CT15GENIChomozygous117085028
107291273072912731AT12GENIChomozygous116800098
107291310572913106TC17GENIChomozygous116633288
107291340272913403TC13GENIChomozygous116633290
107291643272916433GA33GENIChomozygous117085032
107291788872917889GA21GENIChomozygous117085034
107291819272918193GT15GENIChomozygous117104619
107291826672918267AG14GENIChomozygous117104621
107291990572919906CT25GENIChomozygous117085036
107292052872920529AT28GENIChomozygous116633294
107292060872920609AC13GENIChomozygous116633296
107292611672926117AC31GENIChomozygous116633300
107292670772926708CT32GENIChomozygous117104623
107292865572928656CT33GENIChomozygous117085044
107293010272930103CT44GENIChomozygous117085046
107293124872931249TG29GENIChomozygous116633304
107293142172931422CT27GENIChomozygous116633306
107293178072931781AT16GENIChomozygous116633308
107293192272931923AG10GENIChomozygous116633310
107293294872932949AG33GENIChomozygous116633312
107293338672933387TC28GENIChomozygous116633314
107293781572937816CT12GENIChomozygous116633324
107294169672941697TG20GENIChomozygous116633326
107294364072943641GA18GENIChomozygous116633334
107294411872944119GT24GENIChomozygous116633336
107294442472944425TC16GENIChomozygous116633338