chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
107502331275023313GGC23GENIChomozygous51497831
107502392275023923GA23GENIChomozygous51497832
107502523675025237GA38GENIChomozygous51497833
107502533475025335TC37GENIChomozygous51497834
107502656175026562GA29GENIChomozygous51497835
107502656375026564GC27GENIChomozygous51497836
107502690175026902TC20GENIChomozygous51497837
107502700275027003AG18GENIChomozygous51497838
107502734675027347AG12GENIChomozygous51497839
107502837475028395CAAACAAACAAACAAACAACC---------------------17GENICheterozygous52386158
107502837875028394CAAACAAACAAACAAC----------------11GENICheterozygous52804474
107503130575031306GT30GENIChomozygous51497842
107503187175031872GGCC8GENICheterozygous51497843
107503187175031872GGC8GENICheterozygous51497844
107503223675032237CT32GENIChomozygous51497845
107503281975032857CCTGCAGCAGCTGCAGCTGGGACACCTCCACCAGCACA--------------------------------------4GENIChomozygous52386160
107503447675034477CCT28GENIChomozygous51497846
107503466075034792GGGCTGGGGATTTAGCTCAGTGGTAGAGCGCTTACCTAGGAAGCGCAAGGCCCTGGGTTCGATCCCCAGCTCCGAAAAAAAGAACCAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGAATGGGGATCCTTAA------------------------------------------------------------------------------------------------------------------------------------14GENIChomozygous52321309
107503513275035133AAACACACAC2GENIChomozygous52683054
107503553075035531AAACACACACACACACCTCACAAACAC10GENICpossibly homozygous52804477
107503587675035877AC17GENIChomozygous51497853
107503589375035894C-17GENIChomozygous51497854
107503682275036823GA48GENIChomozygous51497855
107503867675038677TTG22GENIChomozygous51497856
107503889675038902ACACAT------13GENICheterozygous52804480
107504201075042011C-33GENIChomozygous51497858
107504333075043331TC27GENIChomozygous51497859
107504759775047631TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG----------------------------------23GENIChomozygous52386164
107504765275047654GA--21GENIChomozygous51497861