chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
107519609975196100G-34GENIChomozygous699469732
107519701475197015TC29GENIChomozygous550249951
107519744275197443TC17GENIChomozygous550249952
107519886475198865AG26GENIChomozygous550249953
107520110875201109CT18GENIChomozygous552035736
107520167575201676A-6GENICheterozygous699469733
107520670675206707CCTCTCTCTCTCTCTT17GENICheterozygous699469734
107520672975206737TCTCTCTC--------4GENIChomozygous699469737
107520689775206909AGTGGCAGTGGC------------22GENIChomozygous699469739
107520781175207812TC29GENIChomozygous552035737
107520806775208068CCT12GENICheterozygous699469740
107520816075208161AG27GENIChomozygous552035738
107520817675208177TC34GENIChomozygous552035739
107520930575209306TC40GENIChomozygous552035740
107521038575210386TC37GENIChomozygous550249954
107521095775210958GC24GENIChomozygous552035741
107521109975211100GA31GENIChomozygous552035742
107521167075211671AAG10GENICheterozygous699469741
107521167075211671AAGG10GENICpossibly homozygous699469742
107521207075212072AG--36GENIChomozygous699469743
107521219375212194GA29GENIChomozygous552035743
107521260675212607GT8GENIChomozygous552035744
107521283875212839CCCA26GENIChomozygous699469744
107521307575213076AAT23GENIChomozygous699469745
107521309275213093GC21GENIChomozygous550249955
107521405075214051AATT26GENICpossibly homozygous699469746