chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1267608136267608137T21GENIChomozygous132543628
1267609760267609761A25GENIChomozygous132543629
1267608872267608873GC18GENIChomozygous109028864
1267608952267608953GA21GENIChomozygous109028865
1267609159267609160CT16GENIChomozygous109028866
1267609841267609842GA16GENIChomozygous109028867
1267609504267609505CA23GENIChomozygous108785144
1267610232267610233AG20GENIChomozygous108785147
1267610507267610508CT16GENIChomozygous108785149
1267610670267610671CT16GENIChomozygous108785150
1267610679267610680TC16GENIChomozygous108785151
1267610699267610700TG13GENIChomozygous109028868
1267610757267610758AG15GENIChomozygous108785152
1267610775267610776CT15GENIChomozygous108785153
1267610875267610876GT17GENIChomozygous108785154
1267611057267611058CT18GENIChomozygous108785156
1267611752267611753GA4GENIChomozygous108785157
1267612073267612074GA19GENIChomozygous108785158
1267612324267612325AG24GENIChomozygous108785159
1267612713267612832GATTTCTGATATATCTTTTTTTTTTTTTTTTTGGTTCTTTTTTTCGGAGCTGGGGACCGAACCCAGGGCCTTGCGTTTCCTAGGTAAGCGCTCTACCACTGAGCTAAATCCCCAGCCCC9GENICheterozygous131268126
1267612916267612917TG25GENIChomozygous109028869
1267613315267613316AG23GENIChomozygous108640330
1267613496267613497GA22GENIChomozygous109028870
1267613599267613600TC21GENIChomozygous108640331
1267614130267614131C23GENIChomozygous127509630
1267614470267614471GA8GENIChomozygous108640332
1267615245267615246GA28GENIChomozygous109028871
1267615309267615309TGG28GENIChomozygous131268127
1267615547267615549CG25GENIChomozygous127509631
1267615641267615642AG33GENIChomozygous108640334
1267616271267616272AT25GENIChomozygous109028872
1267616624267616624GTTT13GENIChomozygous130835777
1267616674267616675CG7GENIChomozygous109028873
1267616965267616965ACC10GENIChomozygous130835778
1267617221267617222CT17GENIChomozygous109028874
1267611746267611747AG9GENICheterozygous134325011
1267611749267611749TGTGTGTGT9GENICheterozygous134322241