chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
75494457154944572A-13GENICpossibly homozygous55661458
75494505654945057CT6GENIChomozygous55661460
75494517954945180CT22GENIChomozygous55661463
75494581654945817CT27GENICpossibly homozygous55661465
75494593954945940GA22GENIChomozygous55661467
75494609854946099GA19GENIChomozygous54195886
75494690554946906CT16GENIChomozygous55661469
75494802954948030GA21GENIChomozygous55661471
75494805254948053CT19GENICpossibly homozygous55661474
75494869054948691G-6GENIChomozygous55564801
75495091154950912CT10GENIChomozygous55661476
75495172854951729A-3GENIChomozygous55661478
75495200354952004AT18GENIChomozygous53928879
75495276354952764CT5GENIChomozygous55661480
75495651054956511CT1GENIChomozygous55661482
75495660954956610AC1GENIChomozygous53928901
75496080254960803TC21GENIChomozygous53928920
75496178654961787AG24GENIChomozygous55661484
75496241354962414AAG10GENIChomozygous53928926
75496241554962416AAG10GENIChomozygous53928928
75496308054963081CA13GENIChomozygous53928930
75496413754964138CT7GENIChomozygous53928931
75496458454964585CT21GENICpossibly homozygous53928933
75496806054968061TC7GENIChomozygous53928936
75496833454968335TC17GENIChomozygous53928938
75496850354968504AAAACAAC1GENIChomozygous55355442
75496024354960244T-4GENIChomozygous55469504
75496862754968628AC13GENIChomozygous55661488
75496896654968967TC15GENIChomozygous53928940
75496936954969370CT15GENICpossibly homozygous53928942
75496989654969897GA11GENIChomozygous53928945
75497030454970305TTA15GENICpossibly homozygous53928949
75497087854970879AC5GENICheterozygous55564837
75497310154973102TG10GENIChomozygous55661492
75497420754974208AAAAAC17GENICheterozygous54902819