chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1267608872267608873GC52GENIChomozygous109028864
1267608952267608953GA52GENIChomozygous109028865
1267609159267609160CT32GENIChomozygous109028866
1267609504267609505CA34GENIChomozygous108785144
1267609841267609842GA26GENIChomozygous109028867
1267610232267610233AG28GENIChomozygous108785147
1267610507267610508CT20GENIChomozygous108785149
1267610670267610671CT34GENIChomozygous108785150
1267610679267610680TC30GENIChomozygous108785151
1267610699267610700TG28GENIChomozygous109028868
1267610757267610758AG35GENIChomozygous108785152
1267610775267610776CT32GENIChomozygous108785153
1267611057267611058CT31GENIChomozygous108785156
1267612073267612074GA36GENIChomozygous108785158
1267612324267612325AG31GENIChomozygous108785159
1267612916267612917TG31GENIChomozygous109028869
1267613315267613316AG26GENIChomozygous108640330
1267613496267613497GA38GENIChomozygous109028870
1267613599267613600TC30GENIChomozygous108640331
1267614470267614471GA22GENIChomozygous108640332
1267615245267615246GA36GENIChomozygous109028871
1267615641267615642AG22GENIChomozygous108640334
1267616271267616272AT28GENIChomozygous109028872
1267617221267617222CT22GENIChomozygous109028874