chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8107827037107827038CT17GENIChomozygous116986151
8107827353107827354TG5GENICheterozygous126688885
8107827950107827951CT6GENIChomozygous116632870
8107828356107828357AG28GENIChomozygous116986153
8107828560107828561TC24GENIChomozygous116632874
8107829040107829041AG14GENIChomozygous116986154
8107829945107829946GA27GENIChomozygous116986155
8107830412107830413GA19GENIChomozygous116986156
8107830434107830435GT23GENIChomozygous116986157
8107830684107830685AC17GENIChomozygous116986158
8107831300107831301CT9GENIChomozygous116986159
8107831341107831342TC14GENIChomozygous116986160
8107832023107832024GA6GENIChomozygous126724590
8107832145107832146GA17GENIChomozygous116986161
8107832158107832159CT17GENIChomozygous116986162
8107832496107832497CT21GENIChomozygous116986163
8107832719107832720AG19GENIChomozygous116986164
8107832904107832905AG19GENIChomozygous116632878
8107833474107833475AG26GENIChomozygous116986165
8107834093107834094CA25GENIChomozygous116986166
8107834695107834696TA10GENIChomozygous116986167
8107834757107834758CT10GENIChomozygous116986168
8107834834107834835CG4GENIChomozygous116986169
8107835695107835696TC13GENIChomozygous116632888
8107835789107835790GA14GENIChomozygous116986170
8107836840107836841TC4GENIChomozygous116632892
8107836933107836934TC13GENIChomozygous116986171
8107836977107836978AG6GENIChomozygous116632894