chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1811808501180851CT28GENIChomozygous110568946
1811815541181555AG17GENIChomozygous110512438
1811826531182654GA26GENIChomozygous110512441
1811865781186579CT36GENIChomozygous110568951
1811870671187068CG31GENIChomozygous110512443
1811883021188303AT21GENIChomozygous110512445
1811885051188506TC21GENIChomozygous110512447
1811887311188732GA29GENIChomozygous110512449
1811888461188847AG25GENIChomozygous110512452
1811889311188932AG12GENIChomozygous110512454
1811904481190449GC34GENIChomozygous110512456
1811930431193044AG14GENIChomozygous110512458
1811954301195431CG16GENIChomozygous110568954
1811954361195437TC17GENIChomozygous110568956
1811978511197852TC25GENIChomozygous110512462
1811864011186402C36GENICheterozygous129504520
1811820651182067GA8GENICheterozygous131754992
1811896661189667T25GENIChomozygous131202388
1811916391191640TG17GENIChomozygous110619479
1812001391200140AG33GENIChomozygous110568959
1812001741200174CTC35GENIChomozygous131202390
1812005281200529TA22GENIChomozygous110512464
1812005981200599TA22GENIChomozygous110512466
1812018631201864AG35GENIChomozygous110568961
1812022861202287AC32GENIChomozygous110512468
1812029971202998TG25GENIChomozygous110512472
1812039991204000T23GENIChomozygous131202391
1812047151204716CA28GENIChomozygous110512479
1812057161205717CT29GENIChomozygous110568964
1812076001207601AC22GENIChomozygous110512481
1812094141209416AC14GENICpossibly homozygous131202392
1812095061209506A25GENIChomozygous131202393
1812097071209707C23GENIChomozygous131202394
1812129671212968GA25GENIChomozygous110568966
1812155651215566AT22GENIChomozygous110512487
1812117201211721A9GENIChomozygous131202395
1812127171212717AGGGAAAAAAGAAGGC19GENIChomozygous131202396