chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1202159614202159615GT16GENIChomozygous135789993
1202159683202159684AG17GENIChomozygous135789994
1202159712202159713TC22GENIChomozygous135789995
1202160007202160008AG14GENIChomozygous135789996
1202160777202160778TG28GENIChomozygous135789997
1202161032202161033TC22GENIChomozygous135789998
1202161827202161828AG20GENIChomozygous135789999
1202161858202161859TC20GENIChomozygous135790000
1202162253202162254CA15GENIChomozygous135790001
1202162375202162376T13GENICpossibly homozygous135455135
1202162399202162400T13GENIChomozygous135455136
1202162413202162414CT13GENIChomozygous135790002
1202164111202164112CT30GENIChomozygous135790003
1202164197202164198AG25GENIChomozygous135790004
1202164416202164417CT15GENIChomozygous135790005
1202165130202165131CG20GENIChomozygous135790006
1202166664202166672GTGTGTGC17GENIChomozygous135455137
1202167366202167367CT17GENIChomozygous135790007
1202167805202167806GA16GENIChomozygous135790008
1202168250202168251CA19GENIChomozygous135790009
1202168266202168267GT16GENIChomozygous135790010
1202169316202169317TC15GENIChomozygous135790014
1202168385202168386GC18GENIChomozygous135790011
1202168484202168485TC26GENIChomozygous135790012
1202168941202168942AG17GENIChomozygous135790013
1202169656202169657GA23GENIChomozygous135790015
1202172862202172863GC18GENIChomozygous135790016
1202172949202172950AT23GENIChomozygous135790017
1202174562202174563CA25GENIChomozygous135790018
1202169639202169639G19GENIChomozygous135455138