chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121747450417474505GA16GENIChomozygous115273906
121747464017474641AG22GENIChomozygous115273908
121747560317475604GA16GENIChomozygous115483545
121747796217477963AT23GENIChomozygous115273912
121747803117478032CG21GENIChomozygous115273914
121747912217479123TC10GENIChomozygous115273916
121747924617479247CT4GENIChomozygous115273918
121747972017479721CT23GENIChomozygous115273920
121747975217479753CT21GENIChomozygous115273922
121748013717480138GA30GENIChomozygous115483546
121748099517480996TC17GENIChomozygous115273924
121748106817481069CT23GENIChomozygous115483547
121748111417481115TC25GENIChomozygous115273926
121748134617481347GA19GENIChomozygous115273928
121748156917481570CT32GENIChomozygous115273930
121748170317481704TA35GENIChomozygous115273932
121748176317481764CT26GENIChomozygous115273934
121748207317482074GA20GENIChomozygous115273936
121748246517482466AG28GENIChomozygous115273938
121748249617482497TC31GENIChomozygous115273940
121748329817483299CT22GENIChomozygous115273942
121748366617483667AC18GENIChomozygous115273944
121748385917483860AG11GENIChomozygous115273946
121748392517483926TC4GENIChomozygous115273948
121748440817484409CA8GENIChomozygous115273950
121748442817484429CT8GENIChomozygous115273952
121748562717485628TC9GENIChomozygous115273954
121748564017485641AG10GENIChomozygous115273956
121748572317485724TA4GENIChomozygous115273958
121748629717486298AG10GENIChomozygous115273960