chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1811788401178841GA16GENICheterozygous134352830
1811820651182067GA6GENICheterozygous131754992
1811808501180851CT23GENIChomozygous110568946
1811865781186579CT17GENIChomozygous110568951
1811815541181555AG10GENIChomozygous110512438
1811826531182654GA22GENIChomozygous110512441
1811870671187068CG13GENIChomozygous110512443
1811864011186402C24GENICheterozygous129504520
1811883021188303AT16GENIChomozygous110512445
1811885051188506TC18GENIChomozygous110512447
1811887311188732GA21GENIChomozygous110512449
1811888461188847AG21GENIChomozygous110512452
1811954301195431CG19GENIChomozygous110568954
1811889311188932AG14GENIChomozygous110512454
1811904481190449GC30GENIChomozygous110512456
1811930431193044AG19GENIChomozygous110512458
1811896661189667T18GENIChomozygous131202388
1811916391191640TG21GENIChomozygous110619479
1811954361195437TC19GENIChomozygous110568956
1811978511197852TC18GENIChomozygous110512462
1812001391200140AG20GENIChomozygous110568959
1812001741200174CTC20GENIChomozygous131202390
1812005281200529TA29GENIChomozygous110512464
1812005981200599TA21GENIChomozygous110512466
1812018631201864AG18GENIChomozygous110568961
1812022861202287AC21GENIChomozygous110512468
1812029971202998TG33GENIChomozygous110512472
1812039991204000T12GENIChomozygous131202391
1812047151204716CA19GENIChomozygous110512479
1812057161205717CT21GENIChomozygous110568964
1812076001207601AC24GENIChomozygous110512481
1812094141209416AC25GENICpossibly homozygous131202392
1812095061209506A29GENIChomozygous131202393
1812097071209707C25GENICpossibly homozygous131202394
1812117201211721A5GENICheterozygous131202395
1812127171212717AGGGAAAAAAGAAGGC20GENIChomozygous131202396
1812129671212968GA30GENIChomozygous110568966
1812155651215566AT14GENIChomozygous110512487