chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
97643361476433615CG26GENICheterozygous53677050
97643367076433671AAT27GENICheterozygous52857843
97643367276433673CCATT30GENICheterozygous53677051
97643367976433680CT29GENICheterozygous53677052
97643371876433719TA26GENICheterozygous52417293
97643372176433722GGC26GENICheterozygous52857845
97644087876440879G-20GENIChomozygous52024926
97645266876452670CA--6GENICheterozygous52243337
97647498176474982CG19GENIChomozygous52024945
97650032676500327GA6GENICheterozygous52024949
97650032676500328GT--6GENICheterozygous52857863
97650033276500333GA6GENICheterozygous53720656
97650708676507087GT20GENIChomozygous52024955
97650709776507098CT19GENIChomozygous52024957
97650715076507151GT17GENIChomozygous52024959
97650718876507189AT20GENIChomozygous52024961
97651366976513670CCT11GENIChomozygous52024963
97651367976513680CCT11GENIChomozygous52024965
97651368376513684CCCA11GENIChomozygous52024967
97652494776524948TTG19GENIChomozygous52024977
97652495676524957TTG16GENIChomozygous52024979
97652497376524974C-19GENIChomozygous52024981
97652498476524985A-19GENIChomozygous52024983
97652500076525001TA14GENIChomozygous52024985
97654135376541354AATC11GENIChomozygous52024989