chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
56195501761955018TC9GENIChomozygous55417551
56195521461955215AG16GENICpossibly homozygous55417553
56195542861955429CT2GENICheterozygous55417555
56195555261955553TC17GENICpossibly homozygous55417557
56195567461955675GT2GENIChomozygous55417563
56195567661955677AG3GENIChomozygous55417565
56195574661955747AG9GENIChomozygous55417567
56195676061956761GT24GENICpossibly homozygous55417571
56195692461956925CT19GENICpossibly homozygous55417573
56195721861957219TC31GENIChomozygous55417575
56195726261957263CT26GENIChomozygous55417577
56195767961957680TC28GENIChomozygous55417579
56195781761957818AG18GENIChomozygous55417581
56195816161958162CT17GENICpossibly homozygous55417583
56195826961958270AC17GENICpossibly homozygous55417585
56195856261958563GGC1GENIChomozygous55417587
56195856561958566TG3GENIChomozygous55417589
56195878861958789GT27GENIChomozygous55417591
56195895361958954TC12GENIChomozygous55417593
56195909761959098TC28GENICpossibly homozygous55417595
56195976861959769CG22GENIChomozygous55417601
56195982761959828CT14GENIChomozygous55417603
56195996661959967CT15GENIChomozygous55417605
56195998361959984TA16GENIChomozygous55417607