chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2185501310185501311CT12GENIChomozygous136407692
2185501321185501322CG11GENIChomozygous136407693
2185501796185501798TA19GENICpossibly homozygous135966844
2185501980185501981AC18GENIChomozygous136407694
2185502703185502704GA21GENIChomozygous136407695
2185502778185502779GT22GENICpossibly homozygous136407696
2185502906185502907GA18GENIChomozygous136407697
2185503660185503661CT13GENIChomozygous136407698
2185504722185504723CT21GENIChomozygous136407699
2185504759185504760GA27GENIChomozygous136407700
2185505351185505352GT16GENIChomozygous136407701
2185506874185506875GA18GENIChomozygous136407702
2185508027185508027AATA19GENIChomozygous135966845
2185508052185508053A24GENIChomozygous135966846
2185509174185509175TA21GENIChomozygous136407706
2185507100185507101GT19GENIChomozygous136407703
2185507373185507374CA32GENIChomozygous136407704
2185508135185508136CT23GENIChomozygous136407705
2185510285185510286GA20GENIChomozygous136407707
2185510354185510355TG15GENIChomozygous136407708
2185510436185510437TC13GENIChomozygous136407709
2185510457185510458CG15GENIChomozygous136407710
2185510473185510474CT16GENIChomozygous136407711
2185510590185510591AG23GENIChomozygous136407712
2185510765185510766GA25GENIChomozygous136407713
2185512088185512089CT16GENIChomozygous136407714
2185514505185514506AG30GENIChomozygous136407715
2185518533185518534GA21GENIChomozygous136407716
2185518800185518801GA22GENIChomozygous136407717
2185518831185518832CG21GENIChomozygous136407718
2185518937185518937AG21GENIChomozygous135966847
2185518966185518967CA21GENIChomozygous136407719
2185519100185519101CT23GENIChomozygous136407720
2185519277185519278TG29GENIChomozygous136407721
2185519405185519406TG20GENIChomozygous136407722
2185519413185519414AG22GENIChomozygous136407723
2185520551185520552CT28GENIChomozygous136407724