chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
151046316710463168GA36GENIChomozygous112896111
151046413710464138GT8GENIChomozygous112896112
151046443510464436G6GENIChomozygous131156604
151046446310464464GA5GENIChomozygous119055669
151046447010464471GA4GENIChomozygous119055670
151046447610464477CG3GENIChomozygous119055671
151046549010465491GT27GENIChomozygous112896113
151046554610465547AC23GENIChomozygous112896114
151046572710465728CT22GENIChomozygous112896115
151046577010465771AG22GENIChomozygous112896116
151046580110465802AG26GENIChomozygous112896117
151046581410465815TG26GENIChomozygous112896118
151046596910465970TC6GENIChomozygous119055672
151046597910465982TCT5GENIChomozygous131156605
151046630910466310CT2GENIChomozygous119055675
151046645410466455TC22GENIChomozygous112981258
151046645310466454TC22GENIChomozygous112981256