chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2209098285209098286CA8GENIChomozygous110814139
2209098288209098289TC8GENIChomozygous110220342
2209098848209098849TA21GENIChomozygous110220343
2209099166209099167GA7GENIChomozygous110220345
2209099168209099169GA7GENIChomozygous110220346
2209099596209099597AC9GENIChomozygous110220350
2209099662209099663TA15GENIChomozygous110220351
2209099680209099681TC13GENIChomozygous110220352
2209099861209099862CT20GENIChomozygous110814141
2209099935209099936GA14GENIChomozygous110220353
2209100005209100006CT7GENIChomozygous110220354
2209100315209100316CT13GENIChomozygous110220355
2209101863209101864GT17GENIChomozygous110220356
2209102263209102264TC16GENIChomozygous110220357
2209103443209103444GA14GENIChomozygous110220361
2209103587209103588AG28GENIChomozygous110220362
2209103758209103759AG19GENIChomozygous110220363
2209104618209104619AT18GENIChomozygous110220365
2209104890209104891CT18GENIChomozygous110220366
2209104902209104903GA19GENIChomozygous110814145
2209105067209105068GA17GENIChomozygous110220368
2209105496209105497AG17GENIChomozygous110220369
2209107100209107101AG19GENIChomozygous110220370
2209107147209107148GT16GENIChomozygous110220371
2209109264209109265TG13GENIChomozygous110220373
2209109518209109519GA18GENIChomozygous110814147
2209109814209109815AT20GENIChomozygous110220374
2209112363209112364CT25GENIChomozygous110814149
2209112376209112377AG23GENIChomozygous110814151
2209112857209112858AG18GENIChomozygous110814153
2209113337209113338AG21GENIChomozygous110220378
2209113399209113400TA20GENIChomozygous110220379
2209113928209113929TC26GENIChomozygous110814155
2209114066209114067AG18GENIChomozygous110814157
2209114563209114564TG11GENIChomozygous110814159
2209114735209114736AC11GENIChomozygous110814161
2209114824209114825AT22GENIChomozygous110814163
2209116304209116305GA17GENIChomozygous110814165