chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
826847492684750T-12GENIChomozygous687663211
826847642684765G-9GENIChomozygous687663212
826848002684801CA9GENIChomozygous515227095
826848012684802CA9GENIChomozygous515227096
826848042684805CT9GENIChomozygous515227097
826848092684810TA9GENIChomozygous515227098
826848102684811GA9GENIChomozygous515227099
826848372684838GGA13GENIChomozygous687663213
826848982684899TA8GENIChomozygous515227100
826849112684912GA13GENIChomozygous515227101
826913372691338T-6GENICheterozygous687663215
826916102691611C-11GENIChomozygous687663216
826918612691862AAT7GENIChomozygous687663217
826920452692046GC31GENICheterozygous515227102
826921192692120AT51GENICheterozygous515227103
826921572692158CG31GENICheterozygous512585038
826922312692232T-24GENICheterozygous687663218
826922412692242CG55GENICheterozygous515227104
826932452693246AT41GENICheterozygous515227105
826932522693253GA44GENICheterozygous515227106
826933062693307GT47GENICheterozygous515227107
826936392693640GT4GENIChomozygous512585039
826962842696285AT11GENIChomozygous515227108
826963602696361CT14GENIChomozygous515227109
827001022700103GGA5GENIChomozygous687663219
827001142700115AAC5GENIChomozygous687663220
827002772700278CCT19GENIChomozygous687663221
827002822700283T-18GENIChomozygous687663222
827079192707920T-20GENICheterozygous687663223