chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
56195501761955018TC52GENIChomozygous55417551
56195521461955215AG33GENIChomozygous55417553
56195542861955429CT22GENICpossibly homozygous55417555
56195555261955553TC19GENIChomozygous55417557
56195565561955657GG--20GENIChomozygous55417559
56195567461955675GT24GENIChomozygous55417563
56195567661955677AG24GENIChomozygous55417565
56195574661955747AG29GENIChomozygous55417567
56195676061956761GT19GENIChomozygous55417571
56195692461956925CT33GENIChomozygous55417573
56195721861957219TC44GENIChomozygous55417575
56195726261957263CT41GENIChomozygous55417577
56195767961957680TC36GENIChomozygous55417579
56195781761957818AG27GENIChomozygous55417581
56195816161958162CT19GENIChomozygous55417583
56195826961958270AC22GENIChomozygous55417585
56195856261958563GGC23GENIChomozygous55417587
56195856561958566TG24GENICpossibly homozygous55417589
56195878861958789GT26GENIChomozygous55417591
56195895361958954TC43GENIChomozygous55417593
56195909761959098TC26GENIChomozygous55417595
56195923961959241TC--10GENIChomozygous55417597
56195924461959247TGT---9GENIChomozygous55417599
56195976861959769CG40GENIChomozygous55417601
56195982761959828CT31GENIChomozygous55417603
56195996661959967CT27GENIChomozygous55417605
56195998361959984TA35GENIChomozygous55417607