chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
9100656336100656337CA13GENIChomozygous52078710
9100656737100656738CT11GENIChomozygous52773471
9100657642100657643AG4GENIChomozygous52078716
9100660408100660409AG7GENIChomozygous52447526
9100656868100656869TC8GENIChomozygous52447516
9100657155100657156AG22GENICpossibly homozygous52447520
9100657368100657369TC13GENIChomozygous52447522
9100660665100660666CT2GENICheterozygous52447528
9100661033100661034GC9GENIChomozygous52447530
9100661269100661270GA2GENIChomozygous52447534
9100661291100661292TC2GENIChomozygous52447536