chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10103657968103657969AG26GENIChomozygous642436687
10103658439103658440AG30GENIChomozygous642436688
10103658665103658666CT30GENIChomozygous642436689
10103659475103659476AC29GENIChomozygous642436690
10103662334103662335C-9GENICpossibly homozygous752572373
10103662601103662602CCT18GENICpossibly homozygous752572374
10103665767103665768AG33GENIChomozygous642436691
10103667623103667624CT31GENIChomozygous642436692
10103667793103667794AG34GENIChomozygous642436693
10103667854103667855AG17GENIChomozygous642436694
10103668206103668210GTGT----23GENIChomozygous752572375
10103668541103668543AA--18GENIChomozygous752572376
10103669968103669969CT27GENIChomozygous642436695
10103670372103670373CT23GENIChomozygous642436696