chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103564102535641026CT16GENIChomozygous116757940
103564196035641961GC10GENIChomozygous126380337
103564201935642020TG5GENIChomozygous126380338
103564208535642086GT6GENIChomozygous126380339
103564624535646246CT18GENIChomozygous116757942
103564782635647827TC22GENIChomozygous116757944
103564795035647951CT15GENIChomozygous116757946
103564822835648229CT19GENIChomozygous116558202
103564934135649342AG6GENIChomozygous116867264
103564959935649600CT5GENIChomozygous116757948
103565216735652168AG9GENIChomozygous116558214
103565278235652783GA9GENIChomozygous116558218
103565310135653102GA15GENIChomozygous116757950
103565316235653163GC22GENIChomozygous116558222
103565521435655215AG8GENIChomozygous116558224
103565562235655623CT10GENIChomozygous116757952
103565728135657282AG8GENIChomozygous116558228
103565744235657443CA9GENICheterozygous116757954
103565812935658130TA5GENICheterozygous116558230
103566001635660017CT22GENIChomozygous116558242
103566117735661178TC19GENIChomozygous116757956
103566191535661916CT12GENIChomozygous116757958
103566279735662798CG6GENIChomozygous116558250
103566592735665928AG8GENIChomozygous116558254
103566717335667174CG4GENICheterozygous126474181
103566773635667737TA15GENIChomozygous116558256
103566807035668071TG10GENIChomozygous116757960
103566829835668299GA19GENIChomozygous116558258
103566831735668318GA18GENIChomozygous116558260
103566953635669537AG6GENICheterozygous118065468
103567125935671260GA21GENIChomozygous116757962
103567257435672575CT18GENIChomozygous116558272
103567276635672767CT19GENIChomozygous116757964
103567296135672962CA11GENIChomozygous116757966
103567313235673133GA10GENIChomozygous116757970
103567313735673138CT10GENIChomozygous116757972
103567350235673503GA19GENIChomozygous116757974
103567358135673582CG19GENIChomozygous116558278
103567415135674152AG13GENIChomozygous116558280
103567466935674670AG12GENIChomozygous116757976