chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
123688003336880033TTG11GENIChomozygous142313778
123688007036880071T7GENIChomozygous139054159
123688185336881854TC15GENICheterozygous154739304
123688185336881854TG15GENIChomozygous154739305
123688241136882413AC6GENIChomozygous142313779
123688264936882655GGGGTG6GENIChomozygous144914744
123688295936882960TC14GENIChomozygous154739306
123688295936882960T14GENICheterozygous403326317
123688434236884343GC23GENIChomozygous142338001
123688259236882593CA11GENIChomozygous139137583
123688813536888136TC13GENIChomozygous139137584
123688394736883948GA19GENIChomozygous142338000
123688865236888659TCTCTCT4GENIChomozygous142313780
123688996536889966CT13GENIChomozygous139137586
123688997136889972CT13GENIChomozygous142338002
123689021536890216GA19GENIChomozygous142338003
123689082536890826AG15GENIChomozygous139137587
123689129836891299GA16GENIChomozygous142338004
123689157136891572TC13GENIChomozygous142338005
123689178236891783AG17GENIChomozygous142338006
123689222336892224GA8GENIChomozygous142338007
123689338036893381GC6GENIChomozygous142338008
123689352436893524A3GENIChomozygous142313781
123689409336894094AG12GENIChomozygous142338009
123689441536894416CT10GENIChomozygous142338010
123689480736894808CT10GENIChomozygous139137591
123689105636891057GA4GENIChomozygous144923679