chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108280280582802806TC13GENIChomozygous116659774
108280419582804196CT17GENIChomozygous116659776
108280439482804395GA12GENIChomozygous116898501
108280441582804416TG5GENIChomozygous126388837
108280444882804449GA7GENIChomozygous116898503
108280445882804459TG5GENIChomozygous126388838
108280447482804475TG5GENIChomozygous126388839
108280457982804580TG6GENIChomozygous126388840
108280458482804585TG7GENIChomozygous126388841
108280458982804590TG6GENIChomozygous126388842
108280459482804595TG6GENIChomozygous126409722
108280461182804612TG7GENIChomozygous126409723
108280464582804646TG7GENIChomozygous126388843
108280465282804653TG8GENIChomozygous126388844
108280466082804661TG10GENIChomozygous126388845
108280585982805860CT14GENIChomozygous116898505
108280633882806339TC28GENIChomozygous116659778
108280700482807005AG13GENIChomozygous116898507
108280710482807105AT15GENIChomozygous116659780
108280784782807848GA18GENIChomozygous116898509
108280974382809744CA4GENICheterozygous126434392
108281147282811473CT21GENIChomozygous116659788
108281340082813401AG23GENIChomozygous116898511
108281366682813667CT25GENIChomozygous116898513
108281406182814062GT11GENICheterozygous116898515
108281416982814170CA17GENIChomozygous116898517
108281425782814258CT18GENIChomozygous116898519
108281468482814685AG14GENIChomozygous116898521
108281577582815776GT16GENIChomozygous126388847
108281618782816188CT21GENIChomozygous116659792