chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6138085996138085998TC--12GENICheterozygous54753932
6138086029138086030AG11GENICpossibly homozygous54753934
6138086040138086041CT12GENIChomozygous54753936
6138086150138086151TA16GENICheterozygous54753938
6138086254138086255CT10GENIChomozygous54753942
6138086325138086326GA20GENIChomozygous54753944
6138086349138086350CT15GENIChomozygous54753946
6138086399138086400AG14GENIChomozygous54753948
6138086480138086481GGA3GENICheterozygous54753950
6138086675138086676CA7GENIChomozygous54753952
6138086689138086690GT9GENIChomozygous54753954
6138086884138086890GCCTGG------7GENIChomozygous54753956
6138086930138086932AA--4GENIChomozygous54753958
6138086958138086960GT--7GENICpossibly homozygous54753960
6138087384138087385GA9GENICpossibly homozygous54753962
6138087571138087572AG14GENICpossibly homozygous54753964
6138088056138088057AG11GENICheterozygous54753966
6138088359138088360CT17GENICpossibly homozygous54753968
6138088787138088788AAC8GENICheterozygous54753970
6138089057138089058TC13GENICheterozygous54753973
6138090953138090954AG22GENICpossibly homozygous54753977