chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7121216039121216040TC26GENICpossibly homozygous116225113
7121216967121216968TG18GENIChomozygous116225114
7121216978121216979GA15GENIChomozygous118418033
7121217552121217553AG27GENICpossibly homozygous118418034
7121218065121218066AG13GENIChomozygous118418035
7121219627121219628TG17GENIChomozygous116225115
7121221512121221513AG27GENIChomozygous116225116
7121221952121221953AG38GENICpossibly homozygous116225117
7121218535121218536AG30GENIChomozygous115858106
7121223317121223318CT31GENIChomozygous115858110
7121224631121224632GA36GENIChomozygous118321938
7121226093121226094AG20GENIChomozygous115858112
7121227221121227222AG18GENIChomozygous115858114
7121227630121227631AC12GENIChomozygous115858116
7121229029121229030AT25GENIChomozygous115858124
7121231601121231602AG15GENIChomozygous115858130