chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2209098285209098286CA19GENIChomozygous110814139
2209098288209098289TC18GENIChomozygous110220342
2209098848209098849TA23GENIChomozygous110220343
2209099166209099167GA35GENIChomozygous110220345
2209099168209099169GA34GENIChomozygous110220346
2209099596209099597AC17GENIChomozygous110220350
2209099662209099663TA26GENIChomozygous110220351
2209099680209099681TC26GENIChomozygous110220352
2209099861209099862CT23GENIChomozygous110814141
2209099935209099936GA18GENIChomozygous110220353
2209100005209100006CT16GENIChomozygous110220354
2209100315209100316CT24GENIChomozygous110220355
2209101863209101864GT22GENIChomozygous110220356
2209102263209102264TC27GENIChomozygous110220357
2209103443209103444GA23GENIChomozygous110220361
2209103587209103588AG26GENIChomozygous110220362
2209103758209103759AG22GENIChomozygous110220363
2209104618209104619AT18GENIChomozygous110220365
2209104890209104891CT16GENIChomozygous110220366
2209105067209105068GA22GENIChomozygous110220368
2209105496209105497AG23GENIChomozygous110220369
2209107100209107101AG18GENIChomozygous110220370
2209107147209107148GT18GENIChomozygous110220371
2209109264209109265TG21GENIChomozygous110220373
2209109518209109519GA15GENIChomozygous110814147
2209109814209109815AT17GENIChomozygous110220374
2209112363209112364CT9GENIChomozygous110814149
2209112376209112377AG11GENIChomozygous110814151
2209113337209113338AG12GENIChomozygous110220378
2209113399209113400TA5GENIChomozygous110220379
2209113928209113929TC25GENICpossibly homozygous110814155
2209114066209114067AG28GENIChomozygous110814157
2209114563209114564TG24GENIChomozygous110814159
2209114735209114736AC20GENIChomozygous110814161
2209114824209114825AT23GENIChomozygous110814163
2209116304209116305GA20GENIChomozygous110814165