chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7110149989110149990AG22GENICheterozygous54056783
7110150121110150122TC27GENICheterozygous54056784
7110150227110150228TA33GENICheterozygous54056785
7110150237110150238TA28GENICheterozygous54056786
7110162566110162567A-62GENICheterozygous54056829
7110193236110193237CT16GENICheterozygous54223005
7110193437110193438CG14GENICheterozygous54223006
7110200821110200822CT21GENICheterozygous54057000
7110226130110226131CT50GENICheterozygous54057282
7110228151110228152TC12GENICheterozygous54057290
7110277286110277287TC32GENICheterozygous54057431
7110286393110286394GT32GENICheterozygous54499107
7110286746110286747AG66GENICheterozygous56581402
7110286795110286796TC65GENICheterozygous56581403
7110286812110286813CT64GENICheterozygous56581404
7110286917110286918TC60GENICheterozygous54057447
7110287413110287414GC6GENICheterozygous54057448
7110287914110287915CT21GENICheterozygous54499111
7110287969110287970CT26GENICheterozygous54499113
7110288262110288263CA19GENICheterozygous54499119
7110288462110288463GA30GENICheterozygous54499121
7110288719110288720CT23GENICheterozygous54499123