chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1186800896186800897CT16GENIChomozygous76100828
1186801011186801012TC21GENIChomozygous74633146
1186802758186802759GA19GENIChomozygous76100829
1186804394186804395GA16GENIChomozygous74633155
1186806657186806658CT14GENIChomozygous76100830
1186806988186806988T12GENICheterozygous76100831
1186807441186807442GT9GENIChomozygous74633159
1186808141186808142CA18GENIChomozygous76100832
1186808875186808876TA22GENIChomozygous76100833
1186808963186808964TC16GENIChomozygous74633162
1186809526186809527A19GENICheterozygous76100834
1186809527186809528CT17GENICheterozygous76100835
1186811229186811230TC13GENIChomozygous76100836
1186811566186811567CT9GENIChomozygous76100837
1186813244186813245CT16GENIChomozygous76100838
1186813282186813282T17GENICheterozygous76100839
1186814736186814737GA19GENIChomozygous76100840
1186815730186815731AC12GENIChomozygous76100841
1186816720186816721T15GENICheterozygous76100842
1186817009186817009TA8GENICheterozygous76100843
1186817008186817009GA8GENIChomozygous75949323
1186817656186817657GA17GENIChomozygous74633180
1186817732186817733GT20GENIChomozygous74633182
1186819525186819527TA14GENICheterozygous76100844
1186822277186822278TA18GENIChomozygous76100845
1186822751186822752AT15GENIChomozygous74633184
1186825700186825701AT23GENIChomozygous74633186
1186826950186826951GA21GENIChomozygous76100846
1186827924186827925T9GENIChomozygous75949329
1186828556186828557AT29GENIChomozygous74633192
1186829625186829626CA16GENIChomozygous74633193
1186830344186830345GA18GENIChomozygous76100847
1186831330186831331TC12GENIChomozygous74633201
1186832262186832263TG5GENIChomozygous76100848
1186834579186834580AG9GENIChomozygous76100849
1186835189186835190TA6GENIChomozygous76100850
1186836073186836074TG16GENIChomozygous74633213
1186838501186838502GT17GENIChomozygous74633217
1186839774186839775GA12GENIChomozygous76100851
1186840399186840400TA14GENIChomozygous74633219
1186840787186840788AG30GENIChomozygous74633223