chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104749249847492499TC28GENICheterozygous51445946
104749290647492907GA10GENICheterozygous51445947
104749291547492916TC11GENICheterozygous51445948
104749324247493243GA27GENICheterozygous51445949
104749354347493544TC40GENICheterozygous51445951
104749354547493546AAG40GENICheterozygous51445952
104749372647493727GA18GENICheterozygous51445953
104749386547493866TC19GENICheterozygous51445954
104749390847493909TG38GENICheterozygous51445955
104749398147493982GA43GENICheterozygous51445956
104749411347494114CT49GENICheterozygous51445958
104749460147494616GGCTTTAATATCGGA---------------22GENICheterozygous51445962
104749533747495338CT39GENICheterozygous51445969
104749569447495695AG5GENICheterozygous51445970
104749695447496955GA33GENICheterozygous51445974