chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7121216039121216040TC22GENIChomozygous116225113
7121216967121216968TG37GENIChomozygous116225114
7121218535121218536AG36GENIChomozygous115858106
7121219627121219628TG27GENIChomozygous116225115
7121221512121221513AG32GENIChomozygous116225116
7121221952121221953AG28GENIChomozygous116225117
7121224344121224345AG36GENIChomozygous116225118
7121226093121226094AG26GENIChomozygous115858112
7121227095121227096CT34GENIChomozygous116225119
7121227221121227222AG30GENIChomozygous115858114
7121227457121227458TG23GENIChomozygous116225120
7121227468121227469TA25GENIChomozygous116225121
7121229029121229030AT35GENIChomozygous115858124
7121229347121229348CT32GENICheterozygous116225122
7121229351121229352CT32GENICheterozygous116262919
7121231264121231265CA36GENIChomozygous116262920
7121231601121231602AG35GENIChomozygous115858130