chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
135457374054573741AG12GENIChomozygous884307974
135457374454573745CT9GENIChomozygous884307975
135457406054574061TC20GENIChomozygous884307976
135457414954574150AG14GENIChomozygous884307977
135457416954574170GA9GENICheterozygous884307978
135457451054574511TC23GENIChomozygous884307979
135457464054574641GA22GENIChomozygous884307980
135457476154574762GC22GENIChomozygous884307981
135457501954575020TC29GENIChomozygous884307982
135457506354575064GA13GENIChomozygous884307983
135457536054575361GA11GENIChomozygous884307984
135457537054575371GT10GENIChomozygous884307985
135457538654575387AG16GENIChomozygous884307986
135457550754575508GA19GENIChomozygous884307987
135457639654576397TC20GENIChomozygous884307988
135457665554576656AG25GENIChomozygous884307989
135457669254576693CT8GENIChomozygous884307990
135457693754576938AT10GENIChomozygous884307991
135457788454577885CT9GENIChomozygous884307992
135457807954578080CT9GENIChomozygous884307993
135457817754578178TC27GENIChomozygous884307994
135457910154579102AG9GENIChomozygous884307995
135457910654579107TC15GENIChomozygous884307996
135457916754579168GA19GENIChomozygous884307997
135457928754579288GA18GENIChomozygous884307998
135457956354579564AG20GENIChomozygous884307999
135457959354579594TC17GENIChomozygous884308000
135457984654579847GA11GENIChomozygous884308001
135457986954579870AG7GENIChomozygous884308002