chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
191064429810644299GA17GENIChomozygous46059619
191064436510644366TC20GENIChomozygous46059620
191064451610644517CT20GENIChomozygous46059621
191064461310644614CT8GENIChomozygous46059622
191064462210644623AG7GENIChomozygous46059623
191064467310644674TC10GENIChomozygous46059624
191064470510644706GA11GENIChomozygous46059625
191064497310644974CT16GENIChomozygous46059626
191064500010645001CT20GENIChomozygous46059627
191064511110645112TC19GENIChomozygous46059628
191064512910645130GA15GENICheterozygous46059629
191064519710645198AG13GENIChomozygous46059630
191064526210645263TG15GENICheterozygous46486199
191064531110645313CA--11GENICheterozygous46861282
191064567010645671CT9GENIChomozygous46059631
191064597110645972CT10GENICheterozygous46861283
191064605710646058CT9GENIChomozygous46059632
191064611310646114CT13GENICheterozygous46861284
191064621610646217TC18GENIChomozygous46059633
191064626510646266GA10GENICheterozygous46059634
191064627810646279AC8GENICheterozygous46059635
191064637710646378GA10GENIChomozygous46059638
191064673710646738TC11GENIChomozygous46059639
191064674510646746TA14GENIChomozygous46059640
191064678710646788TC13GENICheterozygous46861285
191064718810647202GTGGGGGGGTGGGA--------------7GENICheterozygous46861286
191064740510647406TTC13GENIChomozygous46059643
191064767110647672TC14GENICheterozygous46059644
191064768010647681TC15GENICheterozygous46059645
191064820510648206TG15INTERGENICheterozygous46059646
191065129610651297AC18INTERGENICheterozygous46059650
191065159510651596CT12INTERGENICheterozygous46059651
191065183410651835CT15INTERGENICheterozygous46059653
191065223210652233TG18INTERGENICheterozygous46059658
191065257810652579CA15INTERGENICheterozygous46059659
191065306210653063GA15INTERGENICheterozygous46059660
191065325410653255TC11INTERGENICheterozygous46059661
191065337710653378CA14INTERGENICheterozygous46059662