chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
123610174036101741TA14GENIChomozygous139137401
123610401336104013ATGA14GENICpossibly homozygous142313470
123610487436104875CT1GENIChomozygous146500215
123610488336104884TG1GENIChomozygous146500216
123610489236104896TCTG1GENIChomozygous146499583
123610490636104907T3GENICheterozygous146499584
123610519336105193CTTCCTTT6GENIChomozygous142313471
123610520936105210TC5GENIChomozygous139137403
123610654336106544AC12GENIChomozygous139137405
123610888936108890TC10GENIChomozygous139137408
123610584136105842GA12GENIChomozygous142336685
123610879136108792GC13GENIChomozygous142336686
123610904236109043CT16GENIChomozygous142336687
123610605536106055C10GENIChomozygous139054091