chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1212655812212655813GA28GENIChomozygous520680916
1212658705212658706GA59GENIChomozygous520680917
1212659762212659763TG37GENIChomozygous520680918
1212659968212659969AAT33GENIChomozygous690198176
1212661571212661572GT34GENIChomozygous520680919
1212662522212662523AATT10GENICheterozygous690198177
1212662934212662935T-4GENIChomozygous690198178
1212663465212663466CT48GENIChomozygous520680920
1212664831212664832CT52GENIChomozygous520680921
1212666283212666284AG35GENIChomozygous520680922
1212666736212666737CCAG27GENIChomozygous690198179
1212669279212669280TC37GENIChomozygous520680923
1212669302212669303TA25GENIChomozygous520680924
1212669304212669305AT26GENICpossibly homozygous520680925
1212669743212669744AG61GENIChomozygous520680926
1212670030212670031AG35GENIChomozygous520680927
1212670346212670347CG34GENIChomozygous520680928
1212671116212671117CT37GENIChomozygous520680929
1212671311212671312CT29GENICheterozygous523674722
1212674420212674421GA26GENIChomozygous520680930
1212674751212674752T-36GENIChomozygous690198180
1212676526212676527GA33GENIChomozygous520680931
1212676698212676699GGTTGT29GENIChomozygous690198181
1212680462212680463CT26GENIChomozygous520680932
1212685080212685081GA33GENIChomozygous520680933
1212688791212688792TC41GENIChomozygous520680934