chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
13101476149101476150GT15GENIChomozygous67649697
13101476216101476217CA9GENIChomozygous66168221
13101476217101476218CG9GENIChomozygous66168224
13101476218101476219CG9GENIChomozygous66168227
13101476219101476220CG9GENIChomozygous66168230
13101476220101476221CT8GENIChomozygous66168233
13101477128101477129CT14GENIChomozygous66380630
13101477719101477720GT41GENICpossibly homozygous67649699
13101487413101487414CT13GENICheterozygous66380638
13101487559101487560AT35GENICheterozygous66380640
13101487563101487564CT34GENICheterozygous67649719
13101487884101487885TC16GENICpossibly homozygous67649733
13101487989101487990CA24GENICpossibly homozygous67649735
13101488049101488050CT21GENICpossibly homozygous66168245
13101488073101488074TC17GENICheterozygous67649737
13101488076101488077CT17GENICheterozygous67649739
13101488151101488152CT1GENIChomozygous66168253
13101488172101488173AT3GENIChomozygous66168256
13101488184101488185CT7GENICheterozygous66168259
13101488214101488215TC19GENICpossibly homozygous67649745
13101488426101488427TC19GENIChomozygous66380690
13101488658101488659TC14GENIChomozygous66380694
13101488973101488974AG16GENIChomozygous66380696
13101489312101489313TC13GENICpossibly homozygous67649750
13101489474101489475AG25GENIChomozygous67649752
13101489549101489550GA13GENIChomozygous67649754
13101489573101489574TC14GENIChomozygous66380702
13101489615101489616TG18GENIChomozygous66380704
13101489634101489635TC21GENIChomozygous66380706
13101489857101489858AG31GENIChomozygous66380712
13101489963101489964CT27GENIChomozygous67649756
13101490009101490010TC23GENIChomozygous67649758
13101491025101491026TC20GENIChomozygous67649760
13101491681101491682CT14GENIChomozygous67649762
13101492001101492002GA7GENIChomozygous67649764
13101492016101492017GA7GENIChomozygous67649766
13101492116101492117AG12GENIChomozygous67649768
13101492124101492125AC10GENIChomozygous67649770