chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
89904216399042164TC16GENIChomozygous52751869
89904279299042793AG34GENIChomozygous52751873
89904307899043079GGT19GENICpossibly homozygous53013184
89904312499043125AG35GENIChomozygous53013186
89904313599043136TC34GENIChomozygous52751875
89904361399043614AG25GENIChomozygous53150839
89904370199043702CT24GENIChomozygous53150841
89904571199045712CT19GENIChomozygous52751887
89904746499047465AAAACAACAACAAC35GENIChomozygous52751895
89904807799048078AG26GENIChomozygous53150843
89904662199046633AAATAAATAAAT------------3GENIChomozygous53405465
89905462899054632GTGT----5GENIChomozygous53150845
89905502999055030GA16GENIChomozygous53150847
89905870099058704ACAC----10GENICheterozygous52752034
89905870299058704AC--10GENICheterozygous52752036
89905909599059096TA20GENIChomozygous53150849
89906239499062395TA35GENIChomozygous53150851
89906335799063358AG24GENIChomozygous52752091