chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2209098285209098286CA14GENIChomozygous110814139
2209098288209098289TC14GENIChomozygous110220342
2209098848209098849TA31GENIChomozygous110220343
2209099168209099169GA36GENIChomozygous110220346
2209099166209099167GA36GENIChomozygous110220345
2209099596209099597AC23GENIChomozygous110220350
2209099662209099663TA28GENIChomozygous110220351
2209099680209099681TC35GENIChomozygous110220352
2209099861209099862CT35GENIChomozygous110814141
2209099935209099936GA19GENIChomozygous110220353
2209100005209100006CT16GENIChomozygous110220354
2209100315209100316CT37GENIChomozygous110220355
2209101863209101864GT22GENIChomozygous110220356
2209102263209102264TC22GENIChomozygous110220357
2209103443209103444GA27GENIChomozygous110220361
2209103587209103588AG34GENIChomozygous110220362
2209103758209103759AG31GENIChomozygous110220363
2209104618209104619AT24GENIChomozygous110220365
2209104890209104891CT16GENIChomozygous110220366
2209105067209105068GA30GENIChomozygous110220368
2209105496209105497AG27GENIChomozygous110220369
2209107100209107101AG27GENIChomozygous110220370
2209107147209107148GT24GENIChomozygous110220371
2209109264209109265TG27GENIChomozygous110220373
2209109518209109519GA33GENIChomozygous110814147
2209109814209109815AT27GENIChomozygous110220374
2209112363209112364CT43GENIChomozygous110814149
2209112376209112377AG41GENIChomozygous110814151
2209113337209113338AG27GENIChomozygous110220378
2209113399209113400TA42GENIChomozygous110220379
2209113928209113929TC25GENIChomozygous110814155
2209114066209114067AG25GENIChomozygous110814157
2209114735209114736AC14GENIChomozygous110814161
2209114824209114825AT32GENIChomozygous110814163
2209116304209116305GA27GENIChomozygous110814165