chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1186801011186801012TC22GENIChomozygous74633146
1186801879186801880TC10GENIChomozygous74633149
1186802470186802471AG22GENIChomozygous74633153
1186804394186804395GA39GENIChomozygous74633155
1186807441186807442GT15GENIChomozygous74633159
1186808963186808964TC30GENIChomozygous74633162
1186811846186811847GT10GENIChomozygous75462585
1186803556186803557GT15GENICpossibly homozygous75462577
1186804357186804358CT29GENIChomozygous75462579
1186805596186805597TG23GENIChomozygous75462581
1186812277186812278GT5GENICheterozygous74633170
1186816779186816780TC6GENIChomozygous74633174
1186817656186817657GA15GENIChomozygous74633180
1186817732186817733GT19GENIChomozygous74633182
1186819615186819616CT12GENIChomozygous75462586
1186822751186822752AT16GENIChomozygous74633184
1186825700186825701AT14GENIChomozygous74633186
1186827934186827935GA32GENIChomozygous74633190
1186828556186828557AT22GENIChomozygous74633192
1186828973186828974CT32GENIChomozygous75462588
1186829203186829204CT19GENIChomozygous75462590
1186829625186829626CA19GENIChomozygous74633193
1186831031186831032TC8GENIChomozygous74633197
1186831111186831112AG4GENIChomozygous74633199
1186831330186831331TC5GENIChomozygous74633201
1186831520186831521AG8GENICheterozygous74633207
1186836073186836074TG14GENIChomozygous74633213
1186837487186837488CT15GENIChomozygous75462592
1186838501186838502GT24GENIChomozygous74633217
1186839467186839468AG14GENIChomozygous75462594
1186840399186840400TA14GENIChomozygous74633219
1186840787186840788AG22GENIChomozygous74633223
1186842126186842127AT15GENIChomozygous75462596
1186843235186843236CT14GENICpossibly homozygous74633227
1186843313186843314TC17GENICheterozygous74633229
1186843316186843317CT17GENICheterozygous75462600