chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7122152648122152649GC140GENICheterozygous926231821
7122155180122155181AAG40GENICheterozygous926270151
7122155588122155589CT74GENICheterozygous926231822
7122155717122155718AG90GENICheterozygous926231823
7122155864122155865TC79GENICheterozygous926231824
7122156186122156187CT68GENICheterozygous926231825
7122156212122156213AG73GENICheterozygous926231826
7122156360122156361TC57GENICheterozygous926231827
7122167724122167725GT18INTERGENICheterozygous926231828
7122167763122167764CT19INTERGENICheterozygous926231829
7122167767122167768GA19INTERGENICheterozygous926231830
7122167772122167773TC20INTERGENICheterozygous926231831