chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
123688003336880033TTG12GENIChomozygous142313778
123688185336881854TC18GENICheterozygous154739304
123688185336881854TG18GENIChomozygous154739305
123688241136882413AC13GENIChomozygous142313779
123688295936882960TC5GENICheterozygous154739306
123688007036880071T8GENIChomozygous139054159
123688264936882655GGGGTG5GENIChomozygous144914744
123688295836882960AT5GENICheterozygous144914745
123688295936882960T5GENICheterozygous403326317
123688434236884343GC22GENIChomozygous142338001
123688259236882593CA5GENIChomozygous139137583
123688813536888136TC13GENIChomozygous139137584
123688394736883948GA11GENIChomozygous142338000
123688996536889966CT21GENIChomozygous139137586
123688997136889972CT21GENIChomozygous142338002
123689021536890216GA14GENIChomozygous142338003
123689082536890826AG22GENIChomozygous139137587
123689129836891299GA15GENIChomozygous142338004
123689157136891572TC16GENIChomozygous142338005
123689178236891783AG21GENIChomozygous142338006
123689222336892224GA16GENIChomozygous142338007
123689338036893381GC15GENIChomozygous142338008
123689352436893524A17GENIChomozygous142313781
123689409336894094AG20GENIChomozygous142338009
123689441536894416CT22GENIChomozygous142338010
123689480736894808CT22GENIChomozygous139137591
123689105636891057GA7GENIChomozygous144923679