chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2200594720200594721GC20GENIChomozygous946266505
2200598646200598647CT18GENIChomozygous946266506
2200599051200599052TC18GENIChomozygous946266507
2200599195200599196CA23GENIChomozygous946266508
2200599224200599225CT24GENIChomozygous946266509
2200599675200599676TG19GENIChomozygous946266510
2200599702200599703TG19GENIChomozygous946266511
2200599715200599716AG21GENIChomozygous946266512
2200599757200599758GA21GENIChomozygous946266513
2200600163200600164CT18GENIChomozygous946266514
2200600268200600269CT11GENIChomozygous946266515
2200600342200600343CT13GENIChomozygous946266516
2200601244200601245AG24GENIChomozygous946266517
2200601323200601324TC21GENICpossibly homozygous946266518