chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
107457074474570745AAGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT4GENICheterozygous52321285
107457074474570745AAGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT4GENICheterozygous52461531
107457156674571567GC16GENIChomozygous51696767
107457203174572032CG14GENIChomozygous51912092
107457228874572289CT26GENIChomozygous51912094
107457279174572792C-10GENIChomozygous51496680
107457410774574108AAGT7GENICpossibly homozygous51912096
107457447774574478TTA7GENIChomozygous52461532
107457460974574610GGA13GENIChomozygous51912098
107457466374574665AT--12GENIChomozygous51912100
107457627774576283GTGTGT------6GENICheterozygous52728826
107457628174576283GT--6GENICheterozygous52461533