chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1789011398901140AG10GENIChomozygous1001893433
1789025748902575TC4GENIChomozygous1001893434
1789105788910579GA8GENICpossibly homozygous1001893435
1789111378911138CT7GENIChomozygous1001893436
1789116928911693TC5GENIChomozygous1001893437
1789119388911939CT7GENIChomozygous1001893438
1789122808912281CT6GENIChomozygous1001893439
1789131818913182CT10GENIChomozygous1001893440
1789132948913295GA8GENIChomozygous1001893441
1789139668913967GA6GENIChomozygous1001893442
1789140958914096TA10GENIChomozygous1001893443
1789146588914659AC6GENIChomozygous1001893444
1789147868914787CG10GENIChomozygous1001893445
1789152908915291GA7GENIChomozygous1001893446
1789159048915905AG6GENIChomozygous1001893447
1789168948916895TG7GENIChomozygous1001893448
1789171328917133AG8GENIChomozygous1001893449
1789173048917305TC5GENIChomozygous1001893450
1789175108917511AG3GENIChomozygous1001893451
1789177138917714AG2GENIChomozygous1001893452
1789186958918696GA12GENIChomozygous1001893453
1789187308918731CT12GENIChomozygous1001893454
1789187638918764CT10GENIChomozygous1001893455
1789197478919748TC2GENIChomozygous1001893456
1789202518920252GA4GENIChomozygous1001893457
1789203758920376GA2GENIChomozygous1001893458
1789205728920573AT7GENIChomozygous1001893459
1789205978920598TA8GENIChomozygous1001893460
1789205988920599CG8GENIChomozygous1001893461
1789206118920612AG7GENIChomozygous1001893462
1789225638922564AG3GENIChomozygous1001893463
1789250608925061CT3GENIChomozygous1001893464