chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1211249164211249165AG30GENIChomozygous960043029
1211250496211250497TC28GENIChomozygous960043030
1211250622211250623CG29GENIChomozygous960043031
1211250971211250972AC31GENIChomozygous960043032
1211251987211251988GA26GENIChomozygous960043033
1211252068211252069CT26GENIChomozygous960043034
1211252076211252077AC28GENIChomozygous960043035
1211252203211252204AG17GENIChomozygous960043036
1211254118211254119AT23GENICpossibly homozygous960043037
1211254143211254144CT27GENIChomozygous960043038
1211254145211254146CT27GENIChomozygous960043039
1211254496211254497CT23GENIChomozygous960043040
1211254854211254855CG18GENIChomozygous960043041
1211255440211255441GT22GENIChomozygous960043042
1211255616211255617AT30GENIChomozygous960043043
1211256722211256723TC33GENIChomozygous960043044
1211257074211257075AG35GENIChomozygous960043045
1211258803211258804TC16GENIChomozygous960043046
1211259421211259422AG10GENIChomozygous960043047
1211259737211259738AG32GENIChomozygous960043048
1211260475211260476CG24GENIChomozygous960043049
1211261278211261279AG35GENIChomozygous960043050
1211261430211261431CT34GENIChomozygous960043051
1211262513211262514GA37GENIChomozygous960043052
1211262865211262866AG19GENIChomozygous960043053
1211264098211264099TG23GENIChomozygous960043054