chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
194167659441676595GT24GENICpossibly homozygous109889717
194167917341679174AG55GENIChomozygous109702381
194167938941679390CT40GENIChomozygous109702383
194167954941679550TG40GENIChomozygous109702385
194168005441680054G25GENIChomozygous129609391
194167995741679963TGGGGG19GENIChomozygous129609388
194168003441680034G27GENIChomozygous129609389
194168003641680039TAT27GENIChomozygous129609390
194168005841680059A25GENIChomozygous129609392
194168009241680092CTTGCCA31GENIChomozygous129609393
194168009641680096TGGG37GENIChomozygous129609394
194168012241680122T48GENIChomozygous129609395
194168014341680144C49GENIChomozygous129609396
194168016341680163C49GENIChomozygous129609397
194168027941680280TG51GENIChomozygous109702387
194168032741680328CT52GENIChomozygous109702389
194168067841680679AG52GENIChomozygous109702391
194168100841681009AG35GENIChomozygous109702393
194168134641681350CTAT27GENIChomozygous129609398
194168146041681461AG42GENIChomozygous109702395
194168159641681596TGT34GENIChomozygous129609399
194168165241681660GCCGGGGG25GENIChomozygous129609400
194168166341681768GGGGATTTAGCTCAGTGGTAGAGCGCTTACCTAGGAAGCGCAAGGCCCTGGGTTCGGTCCCCAGCTCCGAAAAAAAGAACCAAAAAAAAAAAAAAAGGACAAGCC26GENIChomozygous129609401
194168218741682188T18GENIChomozygous129609402
194168258541682586TA50GENICpossibly homozygous109702397
194168304441683045CG50GENIChomozygous109702399
194168305241683053AC49GENIChomozygous109702401
194168314441683145CA42GENIChomozygous109702403
194168314841683149TC43GENIChomozygous109702405
194168337441683375TA49GENIChomozygous109702407
194168365641683657A50GENIChomozygous129609403
194168365741683658TG50GENIChomozygous109702409
194168008841680089GA30GENIChomozygous109782225
194168008941680090GA30GENIChomozygous109817114