chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1211249164211249165AG11GENIChomozygous885204107
1211250496211250497TC18GENIChomozygous885204108
1211250622211250623CG20GENIChomozygous885204109
1211250971211250972AC14GENIChomozygous885204110
1211251029211251030TC13GENIChomozygous885204111
1211251057211251058AG13GENIChomozygous885204112
1211251085211251086AC23GENIChomozygous885204113
1211251115211251116TC20GENIChomozygous885204114
1211251536211251537TA14GENIChomozygous885204115
1211252068211252069CT6GENIChomozygous885204116
1211252076211252077AC9GENIChomozygous885204117
1211252203211252204AG12GENIChomozygous885204118
1211252288211252289AC5GENICheterozygous885204119
1211253870211253871CA27GENIChomozygous885204120
1211254118211254119AT21GENIChomozygous885204121
1211254178211254179GA5GENIChomozygous885204122
1211254179211254180GA5GENIChomozygous885204123
1211254496211254497CT17GENIChomozygous885204124
1211255440211255441GT10GENIChomozygous885204125
1211255616211255617AT5GENIChomozygous885204126
1211255691211255692GA21GENIChomozygous885204127
1211256722211256723TC29GENIChomozygous885204128
1211257074211257075AG10GENIChomozygous885204129
1211257599211257600GA17GENIChomozygous885204130
1211258541211258542CT22GENIChomozygous885204131
1211258572211258573GA23GENIChomozygous885204132
1211258803211258804TC6GENIChomozygous885204133
1211259421211259422AG16GENIChomozygous885204134
1211259737211259738AG21GENIChomozygous885204135
1211260475211260476CG15GENIChomozygous885204136
1211261278211261279AG17GENIChomozygous885204137
1211261430211261431CT17GENIChomozygous885204138
1211262513211262514GA9GENIChomozygous885204139
1211262865211262866AG19GENIChomozygous885204140
1211264098211264099TG5GENIChomozygous885204141