chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
137497786974977870AG52GENIChomozygous139344632
137497817574978176TC62GENIChomozygous139344634
137497833874978339CT55GENIChomozygous143593435
137497859874978599CT45GENIChomozygous143593436
137497916874979169AG48GENIChomozygous139344635
137497931874979319AG48GENIChomozygous139344636
137498082174980822CT51GENIChomozygous143593437
137498095174980952TC55GENIChomozygous143593438
137498221074982211CT60GENIChomozygous139344637
137498258174982582GA53GENIChomozygous143593439
137498307674983077CT63GENIChomozygous139344638
137498527474985275GA52GENIChomozygous139344641
137498628274986283AC48GENIChomozygous139344643
137498630374986304TC51GENIChomozygous139344644
137498633574986336AC53GENIChomozygous139344645
137498412274984122T55GENIChomozygous139184584
137498585574985856T51GENICpossibly homozygous139184585
137498073874980739A57GENIChomozygous139184583