chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2143893156143893157GC19GENIChomozygous110038643
2143894274143894275AG22GENIChomozygous110038644
2143894619143894620TC16GENIChomozygous110038645
2143896111143896112CT16GENIChomozygous110038646
2143897555143897556CT15GENIChomozygous110038647
2143901069143901070TC14GENIChomozygous110038648
2143901744143901745CA22GENIChomozygous110038650
2143902388143902389GT35GENIChomozygous110038651
2143902756143902757CT3GENIChomozygous120181136
2143902757143902758TC3GENIChomozygous110761084
2143903272143903273TC33GENIChomozygous110038652
2143904351143904352AG25GENIChomozygous110038653
2143904645143904646AT11GENIChomozygous110038654
2143904653143904654AT11GENIChomozygous110595065
2143905700143905701AG23GENIChomozygous110038655
2143906689143906690TC23GENIChomozygous110038656
2143907569143907570TC14GENIChomozygous110038658
2143908517143908518TC20GENIChomozygous110038659
2143908629143908630TC30GENIChomozygous110038660
2143909585143909586AT19GENIChomozygous110038661
2143909624143909625AG17GENIChomozygous110038662
2143909956143909957TC22GENIChomozygous110038663
2143910190143910191AC22GENIChomozygous110038664
2143911968143911969GA24GENIChomozygous110038665
2143912117143912118AG21GENIChomozygous110038666
2143913467143913468AG23GENIChomozygous110038667
2143914528143914529TC10GENIChomozygous110038668
2143916086143916087CA23GENIChomozygous110038669
2143916299143916300TA22GENIChomozygous110038670
2143916356143916357AG25GENIChomozygous110038671
2143918460143918461AC19GENIChomozygous110038672
2143920791143920792GA19GENIChomozygous110038674
2143921193143921194TC22GENIChomozygous110038675
2143922849143922850GA22GENIChomozygous110038676
2143923212143923213TG14GENIChomozygous110038677
2143923832143923833CT24GENIChomozygous110038678
2143923868143923869TA17GENIChomozygous110038679
2143924302143924303CA17GENIChomozygous110038680
2143924414143924415GT12GENIChomozygous110038681
2143917416143917417GT19GENIChomozygous110891205