chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
67375548373755484TTAA6GENIChomozygous684044297
67375646973756470GA15GENIChomozygous502822711
67375707773757078GGT6GENIChomozygous684044299
67375709273757093C-4GENIChomozygous684044300
67375944273759443CT28GENICheterozygous502822712
67375950673759507CT21GENIChomozygous505980199
67375977373759774AAAG31GENIChomozygous684044301
67376005973760062AAA---2GENIChomozygous684044302
67376137973761380CT28GENIChomozygous502822713
67376168073761681AC41GENIChomozygous502822714
67376197773761978CG45GENIChomozygous502822715
67376206773762068TTGGCACTGTGAGAGGCCATG40GENIChomozygous684044303
67376240473762405GC56GENIChomozygous502822716
67376378373763784GA10GENIChomozygous502822717
67376523173765232GT22GENICheterozygous505980200
67376523573765236GC22GENICheterozygous505980201
67376525573765256AG24GENICheterozygous505980202
67376529173765292CT16GENICheterozygous502822718
67376536073765361AG15GENICheterozygous505980203
67376537273765373T-17GENICheterozygous684044304
67376540073765401TC19GENICheterozygous505980204
67376540673765407TG19GENICheterozygous505980205
67376542273765423CG18GENICheterozygous502822719
67376547873765479AC16GENICheterozygous505980206
67376548173765484ATA---15GENICpossibly homozygous684044305
67376558673765587AT24GENIChomozygous502822720
67376603673766037CT38GENIChomozygous502822721
67376606073766061A-32GENIChomozygous684044307
67376649173766492GA18GENIChomozygous502822722
67376691073766911CT33GENIChomozygous502822723
67376741573767416G-16GENIChomozygous684044308
67376741773767418GA23GENICheterozygous505980207
67376742673767429TGG---21GENIChomozygous684044309
67376742773767429GG--21GENIChomozygous684044310
67376742873767433GGTTT-----3GENIChomozygous684044311
67376745473767455CT23GENIChomozygous505980208
67376749073767491AG15GENICpossibly homozygous505980209
67376750073767501CT16GENIChomozygous502822724
67376751873767519GA18GENIChomozygous502822725
67376753073767531AG21GENIChomozygous505980210
67376794273767943GT41GENIChomozygous502822726