chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
135526581055265811CA24INTERGENIChomozygous791019023
135527061455270615AT14INTERGENIChomozygous791019024
135527372555273726AC26GENIChomozygous791019025
135527422555274226CT37GENIChomozygous791019026
135527431555274316AG34GENIChomozygous791019027
135527451255274513AG32GENIChomozygous791019028
135527458955274590CT30GENIChomozygous791019029
135527499255274993CT24GENIChomozygous791019030
135527510155275102GA16GENICpossibly homozygous791019031
135527520655275207AC10GENIChomozygous791019032
135527530955275310AG17GENIChomozygous791019033
135527570255275703CT9GENIChomozygous791019034
135527577555275776TC10GENIChomozygous791019035
135527667255276673GA22GENICpossibly homozygous791019036
135527667555276676TC23GENICpossibly homozygous791019037
135527668755276688GT33GENICheterozygous791019038
135527679555276796TC37GENICheterozygous791019039
135527691155276912GT19GENIChomozygous791019040
135527720255277203AG9GENIChomozygous791019041
135527730555277306AG25GENIChomozygous791019042
135527731055277311GA24GENIChomozygous791019043
135527776155277762CT15GENIChomozygous791019044
135527881855278819GA10GENIChomozygous791019045
135527944755279448TA29GENIChomozygous791019046
135528081355280814GC5GENIChomozygous791019047
135528175455281755CT21GENIChomozygous791019048
135528217055282171CT20GENIChomozygous791019049
135528363155283632TC26GENIChomozygous791019050
135528549255285493TC17GENIChomozygous791019051
135528655655286557GA18GENIChomozygous791019052
135528680955286810AC26GENIChomozygous791019053
135528699155286992AT18GENIChomozygous791019054
135528793355287934AG27GENIChomozygous791019055