chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1851077425107743TG21GENIChomozygous125342871
1851095535109554AG6GENIChomozygous110246524
1851148625114863AG20GENIChomozygous110246530
1851171455117146GT20GENIChomozygous125342872
1851173665117367CA14GENIChomozygous125342873
1851174175117418CT17GENIChomozygous125342874
1851226025122603GT3GENICheterozygous125387412
1851226585122659GT7GENIChomozygous125342875
1851783025178303GC15GENIChomozygous125342878
1851790675179068GC14GENIChomozygous110246651
1851792215179222CA6GENIChomozygous110445318
1851792225179223AC6GENIChomozygous110445319
1851792365179237TA11GENIChomozygous110445320
1851945925194593CT8GENIChomozygous125387413
1852399675239968AT19GENIChomozygous125342880
1852538255253826GA4GENICheterozygous125387414
1852986425298643AT3GENICheterozygous125387415
1853000495300050GA19GENIChomozygous125342884
1853000665300067CG15GENIChomozygous125342885
1853001185300119AT17GENIChomozygous125342886
1853001975300198TG11GENIChomozygous125342887
1853148005314801GA3GENICheterozygous125387416