chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
82788562527885626TC6GENICheterozygous52546144
82788612227886123AG21GENICpossibly homozygous53263497
82788667627886677A-4GENIChomozygous53360078
82788718427887185GA6GENICheterozygous53360079
82788830327888304GA2GENICheterozygous52546146
82788983027889831TC3GENICheterozygous53263502
82789264427892645TC9GENICheterozygous53263509
82790288327902884CG18GENIChomozygous53263536
82790323527903236CT14GENIChomozygous53360080
82790326327903264CA23GENIChomozygous53360081
82790395627903957GT14GENIChomozygous53360082
82790401427904015TA8GENICheterozygous53263540
82790403227904033AG9GENICheterozygous53263541
82790561827905619A-9GENIChomozygous53360083
82790630427906305CT15GENICpossibly homozygous53263548
82790631527906316AT16GENIChomozygous53360084
82790654527906546TC17GENIChomozygous53263549
82790671727906718AAGAGG1GENIChomozygous53360085
82791023827910239AG20GENIChomozygous53263550
82791568627915687TA15GENICpossibly homozygous53360086
82792349727923498AG14GENIChomozygous53360087
82792482027924821AG11GENIChomozygous53360088