chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1200037846200037847CG19GENIChomozygous108502948
1200038390200038393GCA18GENIChomozygous127473217
1200039349200039350TC2GENIChomozygous125307077
1200089413200089413GG15GENIChomozygous127473218
1200090027200090027A17GENIChomozygous127473219
1200091092200091093CT24GENIChomozygous108502954
1200092336200092337TC17GENIChomozygous108502958
1200096126200096127AG19GENIChomozygous109363253
1200100667200100671TTTG11GENIChomozygous127473220
1200101883200101884TA6GENIChomozygous108502964
1200103734200103735CA21GENIChomozygous108502974
1200104065200104066A12GENIChomozygous127473224
1200106263200106264T21GENIChomozygous131581470
1200082176200082176T9GENIChomozygous131581468
1200103869200103870CT18GENIChomozygous120586686
1200104376200104377GA15GENIChomozygous120586688
1200104465200104466CT13GENIChomozygous120586690
1200090493200090494TC13GENIChomozygous120874506
1200091616200091617CA23GENIChomozygous120874507
1200093001200093002GT18GENIChomozygous120874508
1200097462200097463GA5GENIChomozygous131597058
1200107146200107147GA22GENIChomozygous120586694
1200109240200109240TG15GENIChomozygous131581471
1200109746200109746T21GENIChomozygous127473227
1200109793200109794TG22GENIChomozygous120902399
1200110326200110327CA20GENIChomozygous120586698
1200110633200110634CT16GENIChomozygous120874509
1200110639200110640GA16GENIChomozygous120874510
1200110856200110857T11GENICpossibly homozygous127473228
1200111928200111929TC15GENIChomozygous108502988
1200112480200112481AG16GENIChomozygous109363260
1200112530200112531TG16GENIChomozygous109363261
1200112640200112641GA19GENIChomozygous120874511
1200112829200112830AG15GENIChomozygous108502992
1200113046200113053ACCACAC19GENIChomozygous127473230
1200113055200113055G19GENIChomozygous127473231
1200113422200113423TA16GENIChomozygous120874512
1200113468200113469CT29GENIChomozygous120874513
1200115478200115479TC30GENIChomozygous108502998