chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
89904216399042164TC25GENIChomozygous52751869
89904279299042793AG24GENIChomozygous52751873
89904307899043079GGT27GENICheterozygous53013184
89904307899043079GGTT27GENICheterozygous53520979
89904312499043125AG43GENIChomozygous53013186
89904313599043136TC36GENIChomozygous52751875
89904361399043614AG27GENIChomozygous53150839
89904370199043702CT30GENIChomozygous53150841
89904571199045712CT27GENIChomozygous52751887
89904746499047465AAAACAACAACAAC24GENIChomozygous52751895
89904807799048078AG27GENIChomozygous53150843
89905462899054632GTGT----8GENIChomozygous53150845
89905502999055030GA18GENIChomozygous53150847
89905909599059096TA23GENIChomozygous53150849
89906239499062395TA25GENIChomozygous53150851
89906335799063358AG25GENICpossibly homozygous52752091