chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1212655812212655813GA6GENIChomozygous599390157
1212658705212658706GA29GENIChomozygous599390158
1212659762212659763TG27GENIChomozygous599390159
1212659968212659969AAT22GENICpossibly homozygous727474264
1212661571212661572GT38GENIChomozygous599390160
1212662522212662523AAT17GENICheterozygous727474265
1212662522212662523AATT17GENICpossibly homozygous727474266
1212662934212662935T-20GENIChomozygous727474267
1212663465212663466CT17GENIChomozygous599390161
1212664831212664832CT32GENIChomozygous599390162
1212666283212666284AG35GENIChomozygous599390163
1212666736212666737CCAG16GENICpossibly homozygous727474268
1212669279212669280TC23GENIChomozygous599390164
1212669743212669744AG31GENIChomozygous599390165
1212670030212670031AG27GENIChomozygous599390166
1212670346212670347CG37GENIChomozygous599390167
1212671116212671117CT22GENIChomozygous599390168
1212671289212671290CCTT11GENICheterozygous727474269
1212671289212671290CCTTTT11GENICheterozygous727474270
1212674420212674421GA26GENIChomozygous599390169
1212674751212674752T-20GENIChomozygous727474271
1212676526212676527GA29GENIChomozygous599390170
1212676698212676699GGTTGT27GENIChomozygous727474272
1212678348212678351AGG---27GENICheterozygous727474274
1212680462212680463CT33GENIChomozygous599390171
1212681105212681229AAAAACACGTGAGTCCGGGGTTGGGGATTTAGCTCAGTGGTAGAGCGCTTGCCTAGGAAGCGCAAGGCCCTGGGTTCGGTCCCCAGCTCCGGAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA----------------------------------------------------------------------------------------------------------------------------23GENIChomozygous727474275
1212685080212685081GA37GENIChomozygous599390172
1212688791212688792TC34GENIChomozygous599390173