chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
92733412827334129CG19GENIChomozygous117296375
92733427227334273GA11GENIChomozygous117296377
92733431427334315TC12GENIChomozygous117296379
92733439127334392CT14GENIChomozygous117296381
92733469627334697AT12GENIChomozygous117296385
92733696527336966GA26GENIChomozygous117296415
92733728227337283TG27GENIChomozygous117296435
92733734927337350TG23GENICpossibly homozygous117296437
92733742927337430GC7GENIChomozygous117296439
92733755327337554GA20GENIChomozygous117296441
92733784027337841TC16GENIChomozygous117296443
92733785427337855GA20GENIChomozygous117296445
92733893327338934CT15GENIChomozygous117296446
92733894027338941AG12GENIChomozygous117296448
92733896627338967GA12GENIChomozygous117296450
92733905527339056AC7GENIChomozygous117693758