chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1211248249211248250CG43GENIChomozygous778735166
1211249164211249165AG54GENIChomozygous778735167
1211250496211250497TC51GENIChomozygous778735168
1211250622211250623CG67GENIChomozygous778735169
1211250971211250972AC45GENIChomozygous778735170
1211251987211251988GA60GENIChomozygous778735171
1211252068211252069CT38GENIChomozygous778735172
1211252076211252077AC37GENIChomozygous778735173
1211252203211252204AG32GENIChomozygous778735174
1211254118211254119AT72GENIChomozygous778735175
1211254143211254144CT69GENIChomozygous778735176
1211254145211254146CT69GENIChomozygous778735177
1211254496211254497CT55GENIChomozygous778735178
1211254854211254855CG66GENIChomozygous778735179
1211255440211255441GT66GENIChomozygous778735180
1211255616211255617AT44GENIChomozygous778735181
1211256722211256723TC67GENIChomozygous778735182
1211257074211257075AG63GENIChomozygous778735183
1211257451211257452CT62GENIChomozygous778735184
1211258803211258804TC89GENICpossibly homozygous778735185
1211259421211259422AG37GENIChomozygous778735186
1211259580211259581AG3GENIChomozygous778735187
1211259737211259738AG52GENIChomozygous778735188
1211260475211260476CG82GENIChomozygous778735189
1211261278211261279AG50GENIChomozygous778735190
1211261430211261431CT70GENIChomozygous778735191
1211262513211262514GA76GENIChomozygous778735192
1211262865211262866AG39GENIChomozygous778735193
1211264098211264099TG50GENIChomozygous778735194