chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2180898138180898139AG35GENIChomozygous806534455
2180898172180898173GA31GENIChomozygous806534456
2180899056180899057CA36GENICpossibly homozygous806534457
2180899134180899135GA44GENICpossibly homozygous806534458
2180899312180899313AG48GENIChomozygous806534459
2180899631180899632TC36GENIChomozygous806534460
2180899755180899756CT37GENIChomozygous806534461
2180901332180901333TC44GENIChomozygous806534462
2180902408180902409AG45GENICpossibly homozygous806534463
2180903152180903153AT23GENIChomozygous806534464
2180906629180906630AC38GENIChomozygous806534465
2180907151180907152TC47GENIChomozygous806534466
2180907719180907720TA30GENIChomozygous806534467
2180908056180908057TA36GENIChomozygous806534468
2180908111180908112GA37GENIChomozygous806534469
2180910079180910080TC48GENIChomozygous806534470
2180910701180910702AC35GENICpossibly homozygous806534471
2180911479180911480TC47GENIChomozygous806534472
2180911824180911825CG49GENIChomozygous806534473
2180911828180911829GA49GENIChomozygous806534474