chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7123599390123599391CT60GENIChomozygous116082471
7123599399123599400TC60GENIChomozygous116082472
7123599415123599416CT66GENIChomozygous116082473
7123599420123599421CT69GENIChomozygous116082474
7123599707123599708AG55GENIChomozygous115863714
7123599738123599739AG51GENIChomozygous115863718
7123599749123599750CT54GENIChomozygous115863720
7123599765123599766GA53GENIChomozygous116082475
7123600051123600052CT55GENIChomozygous115863724
7123600485123600486CG53GENIChomozygous116082476
7123600610123600611CT61GENIChomozygous115863728
7123601433123601434TC63GENIChomozygous115863730
7123601878123601879GT60GENIChomozygous116082477
7123602044123602045AG68GENIChomozygous115863736
7123602354123602355CA62GENIChomozygous115863738
7123604361123604362AG30GENIChomozygous115863742
7123604744123604745CT37GENIChomozygous116082478
7123605417123605418CT26GENICpossibly homozygous116082479