chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1811808501180851CT21GENIChomozygous110568946
1811815541181555AG14GENIChomozygous110512438
1811826531182654GA22GENIChomozygous110512441
1811840821184083GA4GENIChomozygous110568948
1811865781186579CT16GENIChomozygous110568951
1811870671187068CG16GENIChomozygous110512443
1811883021188303AT23GENIChomozygous110512445
1811885051188506TC17GENIChomozygous110512447
1811887311188732GA14GENIChomozygous110512449
1811888461188847AG15GENIChomozygous110512452
1811889311188932AG15GENIChomozygous110512454
1811904481190449GC11GENIChomozygous110512456
1811930431193044AG19GENIChomozygous110512458
1811954301195431CG22GENIChomozygous110568954
1811954361195437TC22GENIChomozygous110568956
1811978511197852TC28GENIChomozygous110512462
1812001391200140AG27GENIChomozygous110568959
1812005281200529TA16GENIChomozygous110512464
1812005981200599TA17GENIChomozygous110512466
1812018631201864AG18GENIChomozygous110568961
1812022861202287AC13GENIChomozygous110512468
1812029971202998TG20GENIChomozygous110512472
1812047151204716CA25GENIChomozygous110512479
1811916391191640TG12GENIChomozygous110619479
1812028941202895AT11GENIChomozygous110619481
1812057161205717CT11GENIChomozygous110568964
1812076001207601AC21GENIChomozygous110512481
1812117211211722AG13GENICpossibly homozygous110619484
1812129671212968GA15GENIChomozygous110568966
1812155651215566AT25GENIChomozygous110512487
1812150391215040TG21GENICpossibly homozygous110755828